Alifax Holding Spa v. Alcor Scientific Inc. et al

1:14-cv-00440Rid5 de set. de 2019

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UNITED STATES DISTRICT COURT
FOR THE DISTRICT OF RHODE ISLAND
___________________________________
)
ALIFAX HOLDING SPA, 	)
)
Plaintiff, 	)
)
v. 	) 	C.A. No. 14-440 WES
)
ALCOR SCIENTIFIC INC.; and 	)
FRANCESCO A. FRAPPA, 	)
)
Defendants. 	)
___________________________________)
OPINION AND ORDER
WILLIAM E. SMITH, Chief Judge
This intellectual property odyssey came before the Court for
a 	three-week 	jury 	trial 	in 	the 	spring 	of 	2019. 	The 	jury 	found
that 	the 	Defendants 	willfully 	misappropriated 	two 	of 	plaintiff
Alifax 	Holding 	SpA’s 	trade 	secrets 	in 	violation 	of 	Rhode 	Island
law. 	The 	jury 	also 	found 	that 	defendant 	Francesco 	Frappa 	alone
misappropriated a third trade secret and breached his confidential
relationship 	with 	Alifax 	under 	Italian 	law.1 	The 	jury 	awarded
Alifax $6.5 million in unjust enrichment damages. 	Before the Court
are the Defendants’ post-trial motions, which renew their requests
1 	The 	jury’s 	verdict 	concerning 	the 	third 	trade 	secret 	–
“information concerning an anemia factor set forth in exhibits 19
and 	34,” 	see 	Jury 	Verdict 	Form 	Phase 	I: 	Liability, 	ECF 	No. 	292 	–
is not the subject of the pending post-trial motions.
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for 	judgment 	as 	a 	matter 	of 	law2 	and, 	in 	the 	alternative, 	seek 	a
new trial or remittitur.3 	See Alcor’s Mot. for a New Trial, or in
the 	Alternative, 	for 	Remittitur 	(“Mot. 	for 	New 	Trial”),
ECF No. 303; Alcor’s Renewed Mot. for J. As A Matter of Law (“Re-
newed Mot. for JMOL”), ECF No. 304.
Three sophisticated parties aided by experienced counsel and
experts locked horns in this dispute for nearly half a decade. 	In
contrast, 	a 	lay 	jury 	was 	asked 	to 	grasp 	unfamiliar 	technological
and mathematical concepts amid a complex and shifting web of legal
theories in a tiny fraction of that time. 	The Court has calibrated
2 	Frappa’s 	renewed 	request 	for 	judgment 	as 	matter 	of 	law 	on
Count III is considered in a separate order filed contemporaneously
with 	this 	opinion. 	The 	Court 	asked 	for 	supplemental 	briefs 	re-
garding 	whether 	the 	exclusion 	of 	Alifax’s 	theory 	of 	damages 	per-
taining to Frappa individually necessitates a judgment in his favor
on 	Count 	II. 	Trial 	Tr. 	vol. 	11, 	29:19-21, 	May 	1, 	2019. 	Such
briefing never materialized; the parties glibly addressed the is-
sue 	in 	their 	other 	filings. 	The 	Court 	concludes 	that 	the 	Defend-
ants’ liability on Count II is joint and several. Melvin F. Jager,
1 	Trade 	Secrets 	Law 	§ 	3.42, 	at 	n.4.10 	(2019) 	(citing 	cases); 	see
also Salton, Inc. v. Phillips Domestic Appliances & Personal Care
B.V., 	391 	F.3d 	871, 	877 	(7th 	Cir. 	2004); Fishkin 	v. 	Susquehanna
Partners, 	G.P., 	Civil 	Action 	No. 	03-3766, 	2007 	WL 	853769, 	at 	*3
(E.D. Penn. Mar. 19, 2007). 	Thus, Alifax’s untimely disclosure of
its 	theory 	does 	not 	extinguish 	the 	claim 	against 	Frappa. 	As
Frappa’s 	other 	grounds 	for 	judgment 	as 	a 	matter 	of 	law 	were 	co-
extensive 	with 	Alcor’s, 	see Trial 	Tr., 	Vol. 	6, 	110:10-120:4, 	Apr.
24, 	2019, 	the 	Court 	construes 	the 	balance 	of 	Alcor’s 	Rule 	50(b)
motion as a joint motion.
3 	Considering 	the 	Court’s 	rulings 	on 	the 	Defendants’ 	Rule
50(b) motion, the Court accepts Alcor’s invitation to construe its
Rule 59 motion as a joint request from both defendants. 	See Mot.
for New Trial 1, n.1.
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the 	rigor 	of 	its 	post-trial 	assessment 	to 	reflect 	the 	length 	and
complexity of this action.
Regarding the Defendants’ Rule 50(b) motion, the Court finds
that 	Alifax failed to introduce sufficient evidence that using a
clear, plastic photometer sensor (“CPS”) in an ESR analyzer was a
protectable trade secret under the Rhode Island Uniform Trade Se-
crets 	Act 	(“RIUTSA”), 	R.I. 	Gen. 	Laws 	§ 	6-41-1 	et 	seq. 	Thus, 	for
the reasons that follow, the jury’s verdict regarding this theory
of 	liability 	must 	be 	vacated 	and 	judgment 	must 	enter 	for 	the 	De-
fendants. 	The Defendants’ Rule 50(b) motion is otherwise denied.
As 	for 	the 	Defendants’ 	request 	under 	Rule 	59, 	the 	Court 	has
conducted 	an 	exhaustive 	review 	of 	the 	trial 	record. 	Important
policies discourage overturning a jury’s verdict, and there is no
doubt that the jury in this action made a conscientious effort to
find 	the 	facts 	and 	apply 	the 	law. 	Nevertheless, 	after 	a 	careful
examination of evidence, the Court is left with a firm and abiding
conviction 	that 	the 	verdict 	finding 	that 	the 	Defendants’ 	misap-
propriated Alifax’s secret conversion algorithm is contrary to the
clear 	weight 	of 	the 	evidence. 	The 	Court 	is 	similarly 	persuaded
that Alifax’s sole damages witness exceeded the scope permitted by
Federal Rule of Evidence 1006 and that a dramatic trial exhibit (a
prototype 	black 	reading 	cell) 	was 	admitted 	in 	error, 	unfairly
prejudicing the Defendants. 	These findings justify a new trial on
what remains of Count II.
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I. 	Background
The 	legal 	and 	technical 	principles 	that 	drive 	this 	dispute
are 	complex. 	The 	story 	is 	simple.4 	Alifax 	produces 	automated
clinical 	instruments 	that 	are 	used 	to 	determine 	the 	erythrocyte
sedimentation 	rate 	(“ESR”) 	of 	human 	blood 	samples.5 	Francesco
Frappa, an employee of an Alifax subsidiary, departed the company
and 	began 	working 	with 	Alcor, 	a 	Rhode-Island 	based 	competitor.6
Within 	a 	year, 	Alcor 	debuted 	a 	new 	instrument 	– 	the 	iSED 	– 	with
rapid analytical capabilities comparable to Alifax devices. 	This
thunderous litigation ensued.
Alifax has accused Alcor and Frappa of developing the iSED by
pilfering its intellectual property. 	Alifax’s claims included the
following: 	(1) infringement of two patents under 35 U.S.C. § 271;
(2) 	willful 	and 	malicious 	misappropriation 	of 	numerous 	trade 	se-
crets under the Rhode Island Uniform Trade Secrets Act (“RIUTSA”),
R.I. 	Gen. 	Laws 	§ 	6-41-1 	et 	seq.; 	(3) 	breach 	of 	Frappa’s
4 	Only 	the 	context 	for 	the 	Defendants’ 	Rule 	50 	and 	Rule 	59
motions is provided here. 	A more detailed chronicle of particular
chapters from this dispute can be found in the Court’s prior rul-
ings. 	See, e.g., Alifax Holding SpA v. Alcor Sci. Inc, No. CV 14-
440 	WES, 	slip 	op. 	(D.R.I. 	Mar. 	26, 	2019); 	Alifax 	Holding 	SpA 	v.
Alcor Sci. Inc., 357 F.Supp.3d 147 (D.R.I. 2019).
5 	ESR 	is 	a 	common 	clinical 	test 	that 	is 	used 	to 	detect 	non-
specific inflammation.
6 Frappa was employed by Sire Analytical S.r.l. 	During this
litigation, Sire merged completely into Alifax. 	Unless otherwise
noted, the Court refers herein to both entities simply as “Alifax.”
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confidential relationship with Alifax; and (3) copyright infringe-
ment. 	See generally Second Am. & Suppl. Compl., ECF No. 68; Pl.’s
Identification 	of 	Misappropriated 	Trade 	Secrets, 	ECF 	No. 	61-4.
Alcor and Frappa have always denied these contentions. 	Alcor even
counterclaimed, seeking declarations of patent invalidity and al-
leging 	Alifax 	intentionally 	interfered 	with 	its 	prospective 	con-
tractual 	relations. 	Defs.’ 	Ans. 	to 	Pl.’s 	Second 	Am. 	& 	Suppl.
Compl. & First Am. Countercl. (“Ans.”) ¶ 43, ECF No. 71.
The 	parties 	filed 	dispositive 	motions 	targeting 	various
claims in mid-2018. 	In that context, the Court ruled that Italian
law governed the substance of Alifax’s cause of action for breach
of 	a 	confidentiality 	relationship. 	Alifax 	Holding 	SpA 	v. 	Alcor
Sci. 	Inc., 	357 	F. 	Supp. 	3d 	147, 	152 	(D.R.I. 	Jan. 	8, 	2019). 	The
Court 	denied 	the 	Defendants’ 	motion 	for 	summary 	judgment 	on 	the
claims of patent infringement, trade secret misappropriation, cop-
yright infringement, and patent invalidity. 	Alifax Holding SpA v.
Alcor Sci. Inc, No. CV 14-440 WES, slip op. at 40 (D.R.I. Mar. 26,
2019). 	As 	the 	Court 	observed, 	a 	hairsbreadth 	stood 	between 	some
of 	Alifax’s 	claims 	and 	an 	adverse 	result. 	Id. 	Regardless, 	the
Noerr-Pennington doctrine supported summary judgment for Alifax on
Alcor’s intentional interference counterclaim. 	Id.
The 	parties 	tried 	the 	remaining 	claims 	to 	jury 	over 	three
weeks 	in 	April 	and 	May 	2019. 	The 	trial 	was 	bifurcated 	into 	two
phases: 	liability 	and 	damages. 	Prior 	to 	the 	start 	of 	trial, 	the
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Court 	excluded 	the 	copyright-related 	opinion 	of 	Alifax’s 	damages
expert. 	See 	Alifax 	Holding 	SPA 	v. 	Alcor 	Sci. 	Inc., 	C.A. 	No. 	14-
440 	WES, 	2019 	WL 	1579503, 	*1 	(D.R.I. 	Apr. 	12, 	2019). 	Without 	a
theory of damages, the parties agreed that Alifax’s copyright claim
was “out of the case.” 	Trial Tr. vol. 1, 3:10-16, Apr. 15, 2019.
It was not tried to the jury. 	Five days of testimony later, Alifax
expressed 	that 	it 	no 	longer 	wished 	to 	proceed 	on 	its 	patent 	in-
fringement 	claims. 	Trial 	Tr. 	vol. 	5, 	4:7-10, 	Apr. 	22, 	2019.
Without objection from any party, the Court reconsidered its March
26th 	ruling 	and 	granted 	summary 	judgment 	for 	Alcor 	on 	Count 	I 	of
Alifax’s Second Amended Complaint. 	Id. at 77:16-78:7. 	The parties
also 	executed 	a 	covenant 	not 	to 	sue, 	which 	disposed 	of 	Alcor’s
invalidity 	counterclaims. 	Id. 	at 	78:11-79:14. 	Thus, 	at 	the 	end
of the liability phase, the jury deliberated over just two claims:
misappropriation 	of 	trade 	secrets 	and 	breach 	of 	a 	confidential
relationship. 	By 	that 	time 	the 	number 	of 	alleged 	trade 	secrets
had been whittled down to four.
On 	April 	30, 	2019, 	the 	jury 	returned 	its 	verdict. 	The 	jury
found for Alifax, concluding that Alcor and Frappa misappropriated
two of Alifax’s trade secrets:
1. Using 	a 	clear, 	plastic 	capillary 	photometer
sensor 	(“CPS”) 	in 	an 	automated 	ESR 	analyzer,
but only through February 6, 2014; and
2. Portions of computer program source code con-
cerning 	the 	conversion 	of 	photometric
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measurements, 	including 	source 	code 	contain-
ing four specific conversion constants.
Jury Verdict Form Phase I: Liability, ECF No. 292. 	It also found
Frappa (but not Alcor) misappropriated a trade secret comprised of
“[i]nformation concerning an anemia factor . . . ”. 	Id. 	The jury
found 	that 	both 	Defendants 	had 	acted 	willfully 	and 	maliciously.
Id. 	At 	the 	conclusion 	of 	damages 	phase, 	the 	jury 	awarded 	Alifax
$6.5 million in unjust enrichment damages attributable to Alcor’s
misappropriation 	of 	Alifax’s 	source-code 	related 	trade 	secret.7
Jury 	Verdict 	Form 	Phase 	II: 	Damages 	2, 	ECF 	299. 	One 	dollar 	in
nominal 	damages 	was 	awarded 	for 	the 	Defendants’ 	misappropriation
of the CPS-related trade secret.
II. 	Legal Standard
Granting 	judgment 	as 	a 	matter 	of 	law 	to 	overturn 	a 	jury’s
verdict 	is 	warranted 	only 	if 	no 	reasonable 	jury 	could 	have 	found
for 	the 	non-moving 	party. 	Fed. 	R. 	Civ. 	P. 	50; 	Rinsky 	v. 	Cushman
& Wakefield, Inc., 918 F.3d 8, 26 (1st Cir. 2019). 	The Court must
examine the evidence from the nonmovant’s case-in-chief, draw all
reasonable 	inferences 	in 	the 	non-movant’s 	favor, 	and 	determine
7 	The 	Court 	ruled 	that 	the 	jury 	would 	not 	be 	permitted 	to
award 	damages 	based 	on 	Frappa’s 	alleged 	unjust 	enrichment 	as 	an
individual because Alifax failed to adequately disclose that the-
ory 	prior 	to 	trial. 	Trial 	Tr. 	vol. 	11, 	28-29, 	May 	1, 	2019. 	The
Court 	also 	ruled 	that 	Alifax 	would 	be 	held 	to 	its 	representation
that 	it 	was 	only 	seeking 	nominal 	damages 	for 	misappropriation 	of
the CPS-related trade secret.
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whether the verdict has a sufficient evidentiary basis. 	Zimmerman
v. 	Direct 	Fed. 	Credit 	Union, 	262 	F.3d 	70, 	75 	(1st 	Cir. 	2001);
Coyante v. Puerto Rico Ports Auth., 105 F.3d 17, 22 (1st Cir. 1997)
(confining Rule 50 review to “the record upon which the plaintiff
rested 	her 	case 	. 	. 	.”). 	The 	Court 	“may 	not 	consider 	the 	credi-
bility 	of 	witnesses, 	resolve 	conflicts 	in 	testimony, 	or 	evaluate
the weight of the evidence.” 	Barkan v. Dunkin’ Donuts, Inc., 627
F.3d 34, 39 (1st Cir. 2010). 	A verdict cannot be jettisoned with
caprice; the evidence must “point[] unerringly to an opposite con-
clusion.” 	Zimmerman, 	262 	F.3d 	at 	75. 	Nevertheless, 	claims 	built
on 	conjecture, 	speculation, 	or 	a 	“mere 	scintilla” 	of 	evidence 	do
not pass muster. 	Katz v. City Metal Co., 87 F.3d 26, 28 (1st Cir.
1996). 	If 	a 	district 	court 	grants 	a 	renewed 	motion 	for 	judgment
as 	a 	matter 	of 	law, 	it 	must 	make 	a 	conditional 	ruling 	on 	whether
it would grant a new trial if the judgment is later vacated. 	Fed.
R. 	Civ. 	P. 	50(c)(1); 	Jennings 	v. 	Jones, 	499 	F.3d 	2, 	21 	(1st 	Cir.
2007).
A 	trial 	court 	has 	much 	greater 	discretion 	under 	Rule 	59.
Jennings 	v. 	Jones, 	587 	F.3d 	430, 	436 	(noting 	that 	a 	trial 	court
may exercise “broad legal authority” in this context). 	A district
court may order a new trial “whenever, in its judgment, the action
is required in order to prevent injustice.” 	Id. (quotations omit-
ted);
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Ins. 	Co. 	of 	N. 	America 	v. 	Musa, 	785 	F.2d 	370, 	375 	(1st 	Cir.1986)
(stating 	grounds 	for 	a 	new 	trial 	include 	finding 	“the 	verdict 	is
against 	the 	clear 	weight 	of 	the 	evidence, 	is 	based 	upon 	evidence
that is false, or resulted from some trial error and amounts to a
clear 	miscarriage 	of 	justice.”) 	(quotation 	marks 	omitted). 	The
Court is not bound by Rule 50’s strictures. 	It is free to consider
witnesses’ 	credibility, 	independently 	weigh 	the 	proof, 	and 	order
a 	new 	trial 	“even 	where 	the 	verdict 	is 	supported 	by 	substantial
evidence.” 	Jennings, 587 F.3d at 439 (quoting Lama v. Borras, 16
F.3d 	473, 	477 	(1st 	Cir. 	1994)). 	The 	Court 	may 	also 	order 	a 	new
trial 	if 	any 	legal 	or 	factual 	errors 	were 	sufficiently 	grievous
“as 	to 	have rendered the trial unfair.’” 	Astro-Med, 	Inc. 	v.
Plant, 	C.A. 	No. 	06–533 	ML, 	2008 	WL 	4372727, 	*1 	(Sept. 	23,
2008), aff’d 	sub 	nom. Astro-Med, 	Inc. 	v. 	Nihon 	Kohden 	America,
Inc., 	591 	F.3d 	1 	(1st 	Cir. 	2009) 	(quoting 	Parker 	v. 	Town 	of
Swansea, 310 F. Supp.2d 356, 370 (D. Mass. 2004)). 	Still, district
courts must exercise their discretion with caution. 	See Jennings,
587 F.3d at 436 (“[T]rial judges do not sit as thirteenth jurors,
empowered to reject any verdict with which they disagree.”).
Alcor 	has 	also 	asked 	the 	Court 	to 	consider 	an 	alternative
course: 	remittitur. 	If 	the 	court 	finds 	that 	jury’s 	damages 	were
excessive 	or 	contrary 	to 	the 	weight 	of 	the 	evidence, 	a 	district
court may compel a victor to accept either a new trial on damages
or a reduced award. 	See Conjugal P’ship Comprised by Joseph Jones
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& 	Verneta 	G. 	Jones 	v. 	Conjugal 	P’ship 	Comprised 	of 	Arthur 	Pineda
& 	Toni 	Pineda, 	22 	F.3d 	391, 	397 	(1st 	Cir. 	1994); 	see 	also 	Phelan
v. Local 305, 973 F.2d 1050, 1064 (2d Cir.1992). 	A court-ordered
abatement 	is 	justified 	if, 	when 	considered 	in 	the 	most 	favorable
light 	to 	the 	prevailing 	party, 	the 	jury’s 	award 	“exceeds 	any 	ra-
tional 	appraisal 	or 	estimate 	of 	the 	damages 	that 	could 	be 	based
upon the evidence before [the jury].” 	E. Mountain Platform Tennis,
Inc. 	v. 	Sherwin-Williams 	Co. 	Inc., 	40 	F.3d 	492, 	502 	(1st 	Cir.
1994); 	see 	also 	Trainor 	v. 	HEI 	Hosp., 	LLC, 	699 	F.3d 	19, 	32 	(1st
Cir. 2012) (holding remittitur required when evidence was “so thin”
that 	award 	was 	“vastly 	out 	of 	proportion” 	to 	maximum 	recovery
supported 	by 	evidence). 	The 	First 	Circuit 	follows 	the 	“maximum
recovery 	rule.” 	Trainor, 	699 	F.3d 	at 	33. 	Thus, 	any 	remittitur
must 	reflect 	“the 	highest 	reasonable 	total 	of 	damages 	for 	which
there is adequate evidentiary support.” Marchant v. Dayton Tire &
Rubber Co., 836 F.2d 695, 704 (1st Cir. 1988).
III. Discussion
A. 	The Clear, Plastic Capillary Photometer Sensor
Trade Secret
1. 	Alifax 	Did 	Not 	Introduce 	Legally 	Sufficient
Evidence to Support Its Claim That The CPS-Related
Trade Secret Was Protectable Under RIUTSA.
Alcor argues that the Court should vacate the jury’s liability
verdict on Alifax’s CPS-related trade secret claim because Alifax
failed to introduce evidence showing that the first asserted trade
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secret 	– 	“[u]sing 	a 	clear, 	plastic 	capillary 	photometer 	sensor
(“CPS”) 	in 	an 	automated 	ESR 	analyzer” 	– 	satisfied 	RIUTSA’s 	re-
quirements 	for 	protectability. 	See 	Renewed 	Mot. 	for 	JMOL 	4-15.
Alcor 	alternatively 	requests 	a 	new 	trial 	on 	this 	claim. 	See 	Al-
cor’s Mot. for New Trial 4-11. 	The Court agrees on both scores.
RIUTSA defines a “trade secret” in broad terms. 	The statute
protects:
[I]nformation, 	including 	a 	formula, 	pattern,
compilation, 	program, 	device, 	method, 	tech-
nique, or process, that:
(i) 	Derives 	independent 	economic 	value, 	ac-
tual or potential, from not being gener-
ally 	known 	to, 	and 	not 	being 	readily
ascertainable 	by 	proper 	means 	by, 	other
persons 	who 	can 	obtain 	economic 	value
from its disclosure or use; and
(ii) Is 	the 	subject 	of 	efforts 	that 	are 	rea-
sonable under the circumstances to main-
tain its secrecy.
R.I. Gen. Laws § 6-41-1(4). 	The Court required Alifax to disclose
“with 	reasonable 	particularity” 	the 	trade 	secrets 	it 	alleged 	the
Defendants 	misappropriated. 8 	Scheduling 	Order 	¶ 	3, 	ECF 	No. 	36.
This request was not busy work. 	It is a common-sense requirement
8 Such disclosure orders are commonplace in trade secret mis-
appropriation cases. See, e.g., 	DeRubeis v. Witten Techs., Inc.,
244 	F.R.D. 	676, 	681 	(N.D. 	Ga. 	2007) 	(analyzing 	discovery 	consid-
erations 	and 	finding 	“it 	is 	appropriate 	. 	. 	. 	to 	require 	[the
plaintiff] to first identify with ‘reasonable particularity’ those
trade 	secrets 	it 	believes 	to 	be 	at 	issue”); 	BioD, 	LLC 	v. 	Amnio
Tech. LLC, No. 2:13–cv–1670–HRH, 2014 WL 3864658 (D. Ariz. Aug. 6,
2014).
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that furthers the practical needs of discovery and a basic premise
of 	misappropriation 	claims: 	a 	party 	must 	be 	able 	to 	identify 	its
asserted 	trade 	secrets 	with 	reasonable 	specificity. 	See, 	e.g.,
IDX 	Sys. 	Corp. 	v. 	Epic 	Sys. 	Corp., 285 	F.3d 	581, 	583 	(7th 	Cir.
2002); 	Dow Chem. Canada, Inc. v. HRD Corp., 909 F. Supp. 2d 340,
346 (D. Del. 2012); Utah Med. Prods., Inc. v. Clinical Innovations
Assoc., Inc., 79 F. Supp.2d 1290, 1313 (D. Utah 1999), aff’d, 251
F.3d 171 (Fed. Cir. 2000).
Like 	other 	embodiments 	of 	the 	Uniform 	Trade 	Secrets 	Act
(“UTSA”), 	RIUTSA 	does 	not 	protect 	“general 	categories 	of 	infor-
mation” from exploitation. 	Luigino’s, Inc. v. Peterson, 317 F.3d
909, 	912 	(8th 	Cir. 	2003); 	Sarkissian 	Mason, 	Inc. 	v. 	Enter. 	Hold-
ings, 	Inc., 	955 	F. 	Supp.2d 	247, 	255 	(S.D.N.Y. 	2013), aff’d, 572
Fed. 	Appx. 	19 	(2d 	Cir. 	2014). 	To 	show 	a 	protectable 	interest, 	a
plaintiff “must assert specific allegations that it possessed in-
formation 	that 	meets 	the 	definition 	of 	trade 	secret 	under 	[the
act] 	and 	must 	proffer 	evidence 	that 	Defendants 	actually 	received
the trade secret and improperly used it.” 	Sun Media Sys., Inc. v.
KDSM, LLC, 564 F. Supp.2d 946, 965 (S.D. Iowa 2008) (interpreting
language 	of 	Iowa 	UTSA); 	see 	also 	IDX 	Sys. 	Corp., 285 	F.3d 	at 	583
(affirming 	summary 	judgment 	for 	defendants 	on 	misappropriation
claim 	because 	plaintiff 	“failed 	to 	identify 	with specificity the
trade 	secrets 	that 	it 	accuses 	the 	defendants 	of 	misappropriat-
ing.”); 	Imax 	Corp. 	v. 	Cinema 	Techs., 	Inc., 	152 	F.3d 	1161, 	1164
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(9th Cir. 1998) (“A plaintiff seeking relief for misappropriation
of 	trade 	secrets 	‘must 	identify 	the 	trade 	secrets 	and 	carry 	the
burden of showing that they exist.’”).
The uniform statute’s language is the source of this princi-
ple. 	A 	fact 	finder 	cannot 	judge 	whether 	an 	alleged 	trade 	secret
has “independent economic value” if its contours are not reasonably
defined. See R.I. Gen. Laws § 6-41-1(4)(i). 	Nor could one assess
whether such information is not generally known or readily ascer-
tainable. 	See 	Dow 	Chem. 	Canada, 	Inc., 	909 	F. 	Supp. 	2d 	at 	346
(holding 	trade 	secret 	“must 	be 	particular 	enough 	as 	to 	separate
the trade secret from matters of general knowledge in the trade or
of 	special 	knowledge 	of 	persons 	skilled 	in 	the 	trade.”); 	Utah
Med. 	Prods., 	Inc., 	79 	F. 	Supp.2d 	at 	1313 	(concluding 	plaintiff
“must define its claimed trade secret with the precision and par-
ticularity 	necessary 	to 	separate 	it 	from 	the 	general 	skill 	and
knowledge possessed by [defendants].”).
Alifax 	first 	identified 	its 	asserted 	trade 	secrets 	in 	May
2016. 	See 	Pl.’s 	Identification 	of 	Misappropriated 	Trade 	Secrets,
ECF 	No. 	61-4. 	It 	amended 	its 	disclosures 	twice 	over 	the 	ensuing
ten months. 	See Pl.’s First Am. Identification of Misappropriated
Trade 	Secrets, 	ECF 	No. 	61-5; 	Pl.’s 	Second 	Am. 	Identification 	of
Misappropriated Trade Secrets (“Pl.’s Second Disclosure”), ECF No.
137-27. 	The scope of its trade secret claims narrowed further at
summary 	judgment. 	See 	Mem. 	of 	Law 	in 	Opp’n 	to 	Defs.’ 	Mot. 	for
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Partial 	Summary 	J. 	13 	n.2, 	ECF 	No. 	167 	(dropping 	asserted 	trade
secrets 	concerning 	the 	means 	of 	creating 	a 	capillary 	channel 	in
the 	plastic 	CPS 	or 	the 	use 	of 	screws 	with 	Teflon 	washers). 	Each
and 	every 	one 	of 	Alifax’s 	pretrial 	disclosures 	describes 	the 	ma-
terial 	for 	the 	plastic 	CPS 	as 	“a 	single, 	block 	of 	clear 	acrylic”
and 	defines 	the 	component 	as 	a 	“hard 	transparent 	block 	with 	a
capillary channel inside . . . ”. 	Pl.’s Second Disclosure ¶¶ 1-2
(emphasis added).
Based 	on 	Alcor’s 	disclosures, 	the 	Court 	defined 	the 	CPS-re-
lated trade secret at the close of the liability phase as “[u]sing
a 	clear, 	plastic 	capillary 	photometer 	sensor 	(“CPS”) 	in 	an 	auto-
mated ESR analyzer, but only through February 6, 2014.” 	See Ver-
dict Form Phase I: Liability, ECF No. 292; Charge Conf. Tr. 7-11,
Apr. 	26, 	2019, 	ECF 	No. 	345. 	The 	Court 	included 	the 	term 	“clear”
over 	Alifax’s 	objection 	and 	explained 	its 	rationale. 	See 	Charge
Conf. Tr. 7:18-8:17. 	Paragraph 1 of Alifax’s disclosure described
the 	CPS 	as 	a 	“transparent 	block.” 	Pl.’s 	Second 	Disclosure 	¶ 	1.
Paragraph 2 described the CPS as a component made from “a single[]
block 	of 	clear 	acrylic.” 	Id. 	¶ 	2. 	Thus, 	paragraph 	2 	simply
specified the material (clear acrylic) for the “transparent block”
referenced 	in 	paragraph 	1. 	Charge 	Conf. 	Tr. 	10.9 	The 	question
9 	Contrary 	to 	Alifax’s 	argument, 	the 	liability 	phase 	charge
conference was the first time that Alifax suggested it was assert-
ing two separate CPS-related trade secrets. 	See Charge Conf. Tr.
10; 	see 	also 	Mem. 	of 	Law 	in 	Opp’n 	to 	Defs.’ 	Mot. 	for 	Partial
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confronting 	the 	Court 	is 	whether 	the 	evidence 	at 	trial 	can 	be
rationally linked to the identified trade secret (a clear, plastic
CPS).
Viewed 	in 	the 	light 	most 	favorable 	to 	the 	verdict, 	Alifax’s
trial evidence showed that it was developing a CPS that was black
or made of “dark material” to increase its analyzer’s reliability
and reduce maintenance. 	Two witnesses, Giovanni Batista Duic and
Dr. 	Paolo 	Galiano, 	testified 	that 	“La 	Mecca” 	was 	a 	project 	to
improve 	Alifax’s 	instruments 	by 	replacing 	the 	Teflon 	tubing 	with
a 	plastic 	reading 	cell.10 	Trial 	Tr. 	vol. 	2, 	40:7-41:6, 	Apr. 	16,
2019; Trial Tr. vol. 6, 82:21-83:6. 	In 2008, Frappa corresponded
with an Alifax vendor about producing “La Mecca” reading cells by
using a “completely opaque . . . varnish or a thin layer of black
plastic 	material” 	to 	create 	an 	“optical 	shield” 	around 	a 	clear
reading 	cell. 	See 	Trial 	Ex. 	421. 	This 	evidence 	comports 	with
Frappa’s 	account 	of 	“La 	Mecca” 	in 	his 	October 	2011 	technical
Summary J. 12-13 (“the use of a plastic reading cell in a capillary
ESR 	analyzer 	was 	a 	trade 	secret”) 	(“the 	use 	of 	a 	plastic 	reading
cell 	as 	a 	component 	in 	the 	Alifax 	ESR 	analyzer 	was 	not 	generally
known”). 	Alifax pressed that the Court’s characterization of the
asserted trade secret at summary judgment (which was silent as to
CPS’s 	opacity) 	was 	more 	accurate. 	But 	that 	issue 	was 	not 	before
the Court at that time and was not ruled on in the Court’s decision.
The 	question 	at 	summary 	judgment 	was 	whether 	a 	genuine 	dispute
existed 	about 	incorporating 	a 	plastic 	CPS 	into 	an 	ESR 	analyzer.
See Alifax Holding SpA v. Alcor Sci. Inc, No. CV 14-440 WES, slip
op. at 18-20 (D.R.I. Mar. 26, 2019).
10 The terms “reading cell” and CPS are synonymous.
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report. 	See 	Trial 	Ex. 	33. 	It 	describes 	the 	reading 	cell 	as 	a
“block 	of 	dark 	material 	with 	a 	transparent 	area, 	inside, 	[sic]
which 	can 	be 	traversed 	by 	the 	light 	. 	. 	. 	”. 	Id. 	The 	codename
“Mecca” was itself a reference to the reading cell’s dark plastic
material 	(i.e., 	to 	the 	Kaaba 	in 	Mecca, 	Saudi 	Arabia). 	See 	Trial
Tr. 	vol. 	2, 	41:1-8. 	There 	is 	no 	mention 	of 	a 	“clear” 	or 	“trans-
parent” 	reading 	cell. 	Duic 	confirmed 	that 	Frappa’s 	report 	was
“accurate and complete.” 	Id. at 108:23-25.
What 	Duic 	could 	not 	confirm 	was 	that 	Sire 	employed 	Frappa
when 	the 	company 	produced 	both 	clear 	and 	black 	prototype 	reading
cells. 	Trial 	Tr. 	vol. 	2, 	53:4-8. 	He 	affirmed 	– 	at 	most 	– 	that
the prototypes in Fall 2011 were black. 	Id. at 53:11-12. 	Several
days 	later, 	Alifax 	introduced 	a 	tangible 	prototype 	of 	a 	black
reading cell introduced into its analyzers in 2014. 	See Trial Ex.
136. 	Alifax’s 	counsel 	invited 	the 	jury 	to 	compare 	the 	prototype
to 	Alcor’s 	design 	drawings 	for 	a 	plastic 	CPS 	in 	his 	summation.
See id.; Trial Tr. vol. 9, 54:10-11, Apr. 29, 2019.
Alifax 	now 	claims 	that 	the 	color 	of 	the 	CPS 	is 	irrelevant.
Pl.’s 	Opp’n 	to 	Def. 	Alcor 	Sci. 	Inc.’s 	Renewed 	Motion 	for 	J. 	as 	a
Matter of Law (“Opp’n to JMOL”) 6-7, ECF No. 313. 	That cannot be.
Alifax’s asserted trade secret was not the use of any plastic CPS
in 	an 	automated 	ESR 	analyzer. 	It 	was 	the 	use 	of 	a 	plastic 	CPS
that 	was 	“transparent” 	and 	made 	from 	a 	block 	of 	“clear
acrylic.” 	These 	are 	the 	particular 	features 	Alifax 	used 	to
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distinguish its trade secret from general industry knowledge. 	Fur-
thermore, 	Alifax 	contends 	that 	this 	information 	constituted 	a
“combination” 	trade 	secret 	comprised 	of 	public 	domain 	elements.
See Opp’n to JMOL 7; Pl. Alifax Holding SpA’s Opp’n to Def. Alcor
Sci. 	Inc.’s 	Mot. 	for 	a 	New 	Trial, 	or 	in 	the 	Alternative, 	for
Remittitur 	(“Opp’n 	to 	New 	Trial”) 	6, 	ECF 	No. 	314. 	For 	such 	in-
formation to be protectable, the “unified process” resulting from
the 	asserted 	combination 	must 	“afford[] 	a 	competitive 	ad-
vantage.” 	Imperial Chem. Indus. Ltd. v. Natl. Distillers & Chem.
Corp., 	342 	F.2d 	737, 	742 	(2d 	Cir. 	1965). 	In 	other 	words, 	the
elements of the combination trade secret must together create in-
dependent 	economic 	value. 	See, 	e.g., 	Electro-Craft 	Corp. 	v. 	Con-
trolled Motion, Inc., 332 N.W.2d 890, 900 (Minn. 1983) (explaining
that 	independent 	economic 	value 	element 	of 	UTSA 	“carries 	forward
the 	common 	law 	requirement 	of 	competitive 	advantage”); 	Champion
Foodservice, LLC v. Vista Food Exch., Inc., No. 1:13-CV-1195, 2016
WL 	4468001, 	*12 	(N.D. 	Ohio 	August 	24, 	2016) 	(granting 	summary
judgment 	as 	plaintiff 	“advanced 	no 	evidence 	as 	to 	how 	the 	unique
combination 	of 	the 	database 	files—taken 	as 	a 	whole—constitutes
information 	not 	readily 	available 	to 	the 	public 	or 	within 	the
industry, or how this unified combination of information provides
Champion 	with 	a 	competitive 	economic 	advantage 	within 	the 	indus-
try.”)
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Here, evidence of an essential element of the “unique combi-
nation” claimed by Alifax throughout this litigation was missing:
the 	clear 	reading 	cell. 	The 	substance 	of 	Alifax’s 	evidence 	from
its case in chief relates exclusively to the development of a CPS
made from “black” or “dark” material. 	Although Frappa’s May 2008
email 	makes 	passing 	mention 	of 	a 	clear 	reading 	cell, 	the 	same
passage 	refers 	to 	covering 	such 	a 	cell 	in 	“a 	completely 	opaque
layer of varnish or a thin layer of black plastic material . . .”.
See 	Trial 	Ex. 	421. 	This 	speck 	of 	evidence 	cannot, 	by 	itself,
support the conclusion that Alifax was developing a clear reading
cell for use in its ESR analyzers during the relevant time period.
This 	was 	not 	the 	only 	flaw 	in 	Alifax’s 	case 	concerning 	the
CPS-related trade secret. It is well-established that information
that a party can acquire through “normal business channels” is not
protectable. 	APG, Inc. v. MCI Telecomm. Corp., 436 F.3d 294, 307
(1st Cir. 2006) (affirming summary judgment for defendant on mis-
appropriation 	claim 	holding 	disputed 	information 	was 	“obtainable
within normal business channels,” even if acquired by other means);
Rego 	Displays, 	Inc. 	v. 	Fournier, 	379 	A.2d 	1098, 	1101 	(R.I. 	1977)
(stating 	that 	information 	comprises 	a 	trade 	secret 	only 	if 	it
“could not be obtained through public channels”). 	Thus, accepting
for 	argument’s 	sake 	that 	the 	opacity 	of 	the 	CPS 	was 	immaterial,
Alifax 	still 	had 	to 	prove 	that 	its 	CPS-related 	trade 	secret 	was
not 	“generally 	known” 	or 	“readily 	ascertainable 	by 	proper 	means”
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by persons who could “obtain economic value from its disclosure or
use.” 	R.I. 	Gen. 	Laws 	§ 	6-41-1(4)(i); 	see 	also 	Giasson 	Aerospace
Sci., 	Inc. 	v. 	RCO 	Engrg., 	Inc., 	680 	F. 	Supp. 	2d 	830, 	841 	(E.D.
Mich. 	2010) 	(“There 	can 	be 	no 	trade 	secret 	where 	the 	‘secret’ 	is
readily 	ascertainable 	from 	the 	public 	domain.”); 	MicroStrategy
Inc. v. Business Objects, S.A., 331 F. Supp. 2d 396, 416–17 (E.D.
Va. 2004) (“If a competitor could easily discover the information
legitimately, 	the 	inference 	is 	that 	the 	information 	was 	either
essentially ‘public’ or is of de minimus economic value.”).
Again, 	the 	Court 	must 	consider 	the 	evidence 	from 	Alifax’s
case in chief in the light most favorable to the verdict. 	Alifax
elicited testimony that its employees worked on the Mecca project
for several years. 	See Trial Tr. vol. 2, 41:16-24. 	Evidence was
introduced that Alifax worked with a third-party vendor to produce
tangible versions of the CPS component. 	See id. at 41:11-15; Trial
Ex. 	421. 	The jury also heard some testimony concerning measures
intended to maintain the confidentiality of Alifax’s company data,
including that preserving confidentiality was discussed at Alifax
R&D 	meetings; 	the 	company 	used 	generic 	email 	footers 	noting 	that
communications were confidential; and that Alifax provided devices
for 	holding 	company 	data, 	which 	was 	not 	to 	be 	stored 	on 	personal
devices.11 	See Trial Tr. vol. 2, 31:3-17, 35:2-24; Trial Ex. 	20.
11 	The 	parties 	strongly 	dispute 	the 	import 	of 	Alifax’s 	March
2009 	non-disclosure 	agreement 	(“NDA”) 	with 	its 	CPS 	manufacturer,
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Alifax’s 	evidence 	was 	bereft 	of 	additional 	proof 	concerning
ascertainability. 	There was no evidence quantifying the man-hours
or monies expended on developing 	a CPS component.12 	There was no
evidence 	about 	the 	hardware 	found 	in 	ESR 	analyzers 	or 	similar
diagnostic instruments produced by companies other than Alifax or
Alcor. 	There was no evidence about the state of knowledge in the
blood-testing 	or 	clinical 	instrument 	industries 	concerning 	tech-
nologies 	for 	measuring 	optical 	density.13 	Indeed, 	Alifax 	cites
IDEX. 	The Court finds that no juror could have reasonably relied
on this information as probative of any reasonable effort to main-
tain 	the 	confidentiality 	of 	CPS-related 	information. 	The 	record
shows, 	at 	most, 	that 	Alifax 	sent 	CPS-related 	specifications 	to
IDEX almost a year before it executed an NDA and in the absence of
any 	circumstances 	indicating 	that 	IDEX 	was 	obliged 	to 	maintain
their 	confidentiality. 	See 	Trial 	Tr. 	vol. 	2, 	41:9-24, 	108:6-10;
Trial 	Exhibits 	421, 	422; 	see 	also 	Web 	Commc’ns 	Group, 	Inc. 	v.
Gateway 2000, Inc., 889 F. Supp. 316, 320 (N.D. Ill. 1995) (finding
no 	reasonable 	steps 	to 	maintain 	confidentiality 	where 	plaintiff
disclosed 	allegedly 	confidential 	invention 	without 	designating
documents confidential or executing a confidentiality agreement).
12 	Dr. 	Galiano 	testified 	that 	Alifax 	reinvests 	10% 	of 	its
annual profits into research and development activities, but pro-
vided 	no 	details 	concerning 	this 	project. 	See 	Trial 	Tr. 	vol. 	6,
65:24-66:1. 	The Mecca project’s slow progress was also attributed
to Frappa’s limited English proficiency and his responsibility for
“other things.” 	See Trial Tr. vol. 2, 41:24-42:6.
13 Alifax has noted that, on cross-examination during Alcor’s
case, Frappa suggested that an “off-the-shelf” CPS would not work
in 	an 	ESR 	analyzer. 	This 	testimony, 	however, 	does 	not 	explain
whether 	using 	a 	plastic 	CPS 	in 	an 	ESR 	analyzer 	was 	“readily 	as-
certainable” 	in 	the 	industry. 	Furthermore, 	unlike 	at 	summary
judgment, there was no specific evidence at trial that its appli-
cation 	of 	a 	CPS 	was 	novel 	or 	new 	in 	the 	industry. 	See 	Alifax
Holding SpA v. Alcor Sci. Inc, No. CV 14-440 WES, slip op. at 19-
20 (D.R.I. Mar. 26, 2019).
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nothing 	to 	support 	the 	proposition 	in 	its 	briefing 	that, 	before
Frappa joined Alcor, “no other supplier of any type of ESR analyzer
had developed or used a clear plastic CPS.” 	Opp’n to New Trial 8.
Even 	if 	the 	Court 	credited 	that 	statement, 	“[s]imply 	being 	the
first 	or 	only 	one 	to 	use 	certain 	information 	does 	not 	in 	and 	of
itself transform otherwise general knowledge into a trade secret.”
TGC 	Corp. 	v. 	HTM 	Sports, 	B.V., 	896 	F. 	Supp. 	751, 	757 	(E.D. 	Tenn.
1995).
The ruling in Pope v. Alberto-Culver Co., 694 N.E.2d 615, 617
(Ill. App. Ct. 1998) is also instructive.14 	In Pope, an Illinois
appellate 	court 	affirmed 	judgment 	for 	the 	defendant 	on 	a 	trade
secret 	misappropriation 	claim. 	Id. 	at 	619. 	The 	plaintiff’s 	al-
leged 	trade 	secret 	consisted 	of 	a 	lye-based 	hair 	relaxer 	in 	a
squeezable 	tube 	that 	a 	consumer 	could 	use 	to 	spread 	the 	product.
Id. 	at 	616. 	The 	Court 	affirmed 	summary 	judgment, 	agreeing 	that
plaintiff 	failed 	to 	produce 	evidence 	that 	this 	combination 	trade
secret 	was 	not 	comprised 	of 	information 	“generally 	known 	or 	un-
derstood” 	within 	the 	relevant 	industry. 	Id. 	at 	617. 	“[T]he 	key
to secrecy under the Act,” the Court held, “is the ease with which
information 	can 	be 	developed.” 	Id. 	at 	619. 	The 	Pope 	plaintiff’s
asserted 	trade 	secret 	“could 	have 	been 	easily 	and 	cheaply
14 	The 	statutory 	language 	of 	the 	Illinois 	Trade 	Secrets 	Act
is substantially similar to RIUTSA’s terms.
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discovered 	utilizing 	existing 	technology.” 	Id. 	at 	618; 	see 	also
Buffets, Inc. v. Klinke, 73 F.3d 965, 968 (9th Cir. 1996) (recipes
that were “so obvious that very little effort would be required to
‘discover’ them” are not trade secrets).
Here, Alifax was obliged to prove that a “clear, plastic [CPS]
in 	an 	automated 	ESR 	analyzer” 	qualified 	as 	a 	trade 	secret. 	As 	a
court from the District of Kansas explained in Bradbury Co., Inc.
v. 	Teissier-duCros, 	“[t]here 	is 	a 	glaring 	lack 	of 	detail 	showing
any facts about how [the CPS-related trade secret] was not readily
ascertainable 	by 	the 	industry.” 	413 	F. 	Supp. 	2d 	1209, 	1227 	(D.
Kan. 	2006) 	(finding 	plaintiff 	failed 	to 	meet 	burden 	of 	proving 	a
protectable trade secret at summary judgment). 	There was no tes-
timony or documentary proof concerning how difficult, relative to
the 	state 	of 	industry 	knowledge, 	it 	would 	be 	to 	develop 	an 	ESR
analyzer 	that 	measured 	optical 	density 	using 	a 	plastic 	CPS. 	Al-
cor’s generalized development timeline is, in and of itself, una-
vailing. 	See 	Trident 	Prods. 	& 	Servs., 	LLC 	v. 	Canadian 	Soiless
Wholesale, Ltd., 859 F. Supp. 2d 771, 779 (E.D. Va. 2012) (“[E]ven
if a company has expended significant resources to develop a trade
secret 	on 	its 	own, 	it 	cannot 	prevail 	. 	. 	. 	if 	the 	barrier 	to
obtaining that trade secret is quite low in reality.”). 	Thus, for
at 	least 	these 	two 	reasons, 	the 	jury’s 	verdict 	with 	respect 	to
misappropriation of a “clear, plastic CPS” under Count II must be
vacated.
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2. The 	Defendants 	Would 	Be 	Entitled 	to 	A 	New 	Trial 	On
Liability 	for 	Misappropriation 	of 	the 	CPS-Related
Trade Secret.
The 	Court 	would 	grant 	a 	new 	trial 	on 	the 	Defendants’ 	lia-
bility for misappropriating the CPS-related trade secret even ab-
sent 	these 	evidentiary 	shortcomings. 	Upon 	reflection, 	the 	Court
concludes that Trial Exhibit 136 – a prototype black reading cell
introduced by Alifax and produced on the eve of trial – should not
have 	been 	admitted 	into 	evidence. 	Alifax’s 	use 	of 	this 	tangible
evidence unfairly prejudiced Alcor and, by itself, justifies a new
trial.
Alifax first attempted to introduce Trial Exhibit 136 through
Duic. 	See generally Trial Tr. vol. 2, 47-53. 	Alcor objected based
on lack of disclosure. 	Id. at 48-49. 	The Court initially deferred
ruling and gave Alifax an opportunity to lay additional foundation.
Id. 	at 	51:5-11. 	Duic 	testified 	that 	he 	could 	not 	recall 	what
prototypes Frappa worked with and Alifax abandoned its attempt to
admit the exhibit at that time. 	Id. at 53.
Alifax tried again four days later while examining Dr. Gali-
ano. 	See 	Trial 	Tr. 	vol. 	6, 	77-82. 	Dr. 	Galiano 	identified 	the
object 	as 	“the 	device 	called 	MECCA.” 	Id. 	78:11. 	Alcor 	renewed
its objection. 	Id. at 78:3-5. 	Counsel for Alifax explained that
the object “is simply the plastic reading cell which is one of our
trade secret components” and that it was “introduced in 2014” into
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Alifax’s 	products. 	Id. 	at 	79:18-80:2.15 	Counsel 	also 	explained
that (1) Alcor had not specifically requested this object in dis-
covery, and (2) Alcor had an Alifax machine in their office, which
when 	combined 	with 	Frappa’s 	knowledge, 	obviated 	any 	prejudice.
Id. at 80:24-81:9. 	It was undisputed that Alifax had produced the
object 	at 	the 	final 	pretrial 	conference 	and 	that 	Alcor’s 	counsel
photographed 	it. 	Trial 	Tr. 	vol. 	2, 	49:11-50:4. 	The 	Court 	ruled
that the exhibit was admissible for the reasons stated by Alifax’s
counsel. 	Trial Tr. vol. 6, 82:10-13.
The 	Court 	should 	have 	sustained 	Alcor’s 	objection. 	Alcor’s
purported 	failure 	to 	target 	a 	tangible 	version 	of 	the 	disputed
reading 	cell 	in 	its 	discovery 	requests 	is 	irrelevant. 	Rule 	26
requires 	a 	party 	to 	disclose 	“a 	copy 	. 	. 	. 	of 	all 	documents,
electronically 	stored 	information, 	and 	tangible 	things 	that 	the
disclosing 	party 	has 	in 	its 	possession, 	custody, 	or 	control 	and
may use to support its claims or defenses, unless the use would be
solely for impeachment.” 	Fed. R. Civ. P. 26(a)(1)(A)(ii) (emphasis
added). 	A party’s initial disclosures must be made “without await-
ing a discovery request,” Fed. R. Civ. P. 26(a)(1)(A), and must be
supplemented 	“in 	a 	timely 	manner” 	if 	the 	response 	is 	materially
15 	Regarding 	whether 	Trial 	Exhibit 	136 	reflected 	a 	component
Frappa worked on at Sire, Dr. Galiano testified on cross-examina-
tion 	that 	he 	could 	not 	answer 	questions 	about 	“technical 	modifi-
cations” made to Alifax instruments. 	Id. at 88:10-12.
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incomplete and the additional information has not been made known
to 	the 	other 	parties. 	Fed. 	R. 	Civ. 	P. 	26(e)(1)(A). 	If 	a 	party
fails to provide material supplemental information, it may not use
that 	information 	at 	trial 	“unless 	the 	failure 	was 	substantially
justified or is harmless.” 	Fed. R. Civ. P. 37(c)(1).
The physical properties of Alifax’s CPS were always material
to 	its 	trade 	secret 	misappropriation 	claim. 	The 	Court 	also 	has
reason to doubt the contention that the substance of Trial Exhibit
136 	was 	“made 	known” 	to 	the 	Defendants 	through 	their 	acquisition
of one or more Alifax devices. 	Alifax’s counsel represented that
Alifax 	introduced 	the 	CPS 	represented 	by 	the 	exhibit 	into 	its
machines in 2014. 	See Trial Tr. vol. 6, 79:24-25. 	But the depo-
sition testimony of Alcor’s CEO, Carlo Ruggeri, suggests that the
Alifax 	devices 	Alcor 	acquired 	were 	from 	early 	2012. 	See 	Ruggeri
Dep. 	162:1-22.16 	Examining 	machines 	from 	that 	period 	would 	not
have 	revealed 	the 	proffered 	exhibit’s 	substance. 	If 	a 	tangible
version of the CPS existed and Alifax intended to use it at trial,
it 	should 	have 	produced 	it 	during 	discovery. 	It 	neither 	did 	so
nor 	offered 	a 	substantial 	justification 	for 	its 	last-minute 	dis-
closure. 	See Fed. R. Civ. P. 37(c)(1). 	Moreover, when the Court
admitted the prototype, it did not fully appreciate the incongruity
16 	Alifax 	played 	part 	of 	this 	testimony 	for 	the 	jury 	during
its case-in-chief.
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between 	the 	proffered 	exhibit, 	the 	description 	of 	the 	asserted
trade 	secret 	as 	a 	“clear” 	plastic 	block, 	and 	the 	complete 	dearth
of evidence described above. 	With the benefit of 20/20 hindsight,
the correct outcome dictated by these facts is more apparent.
The 	Court 	also 	concludes 	that 	Alifax’s 	failure 	to 	disclose
Trial 	Exhibit 	136 	was 	not 	harmless. 	In 	his 	summation, 	Alifax’s
counsel urged the jury (as he urges the Court post-trial) to infer
misappropriation based on access and substantial similarity. 	See
Trial 	Tr. 	vol. 	9 	49:25-51:10; 	54:3-11; 	Pl.’s 	Opp’n 	to 	New 	Trial
12-13. 	He 	argued 	that 	the 	design 	for 	Alifax’ 	CPS 	“evolved 	into
the 	ultimate 	design 	. 	. 	. 	that’s 	in 	evidence 	as 	Exhibit 	136.”
Trial Tr. vol. 9, 46:18-24. 	He invited the jury to compare Trial
Exhibit 	136 	and 	design 	specifications 	for 	Alcor’s 	reading 	cell,
Trial Exhibit 81, physically placing the tangible object over the
drawings 	using 	the 	Court’s 	document 	camera 	and 	achieving 	a 	com-
pelling 	dramatic 	effect. 	Trial 	Tr. 	vol. 	9, 	50:17-51:9; 	54:3-11.
The 	Defendants, 	on 	the 	other 	hand, 	were 	hamstrung 	by 	their 	ina-
bility 	to 	investigate 	this 	object 	during 	discovery 	and 	challenge
its 	significance. 	Such 	circumstances 	are 	fundamentally 	unfair.
Thus, if the judgment for Alifax were not vacated, the Court would
order 	a 	new 	trial 	on 	liability 	for 	the 	CPS-related 	trade 	secret.
See Astro-Med, 2008 WL 4372727 at *1.
A judge must make snap judgments at trial that are guided by
experience 	and 	instinct 	(and 	often 	based 	on 	imperfect
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information). 	At other times, a judge is afforded time and space
for 	effortful 	deliberation 	and 	reflection. 	To 	borrow 	an 	analogy
offered by an observer of our profession: district judges sometimes
act 	like 	tortoises; 	at 	other 	times, 	they 	must 	act 	like 	hares.17
Rule 	59 	provides 	a 	means 	for 	the 	tortoise 	to 	correct 	the 	hare’s
occasional wrong turns. 	This is one such occasion.
B. 	The 	Conversion 	Algorithm 	Containing 	Four 	Specific
Constants
The 	Court 	has 	remarked 	on 	infirmities 	in 	Alifax’s 	proof 	of
trade 	secret 	misappropriation. 	See, 	e.g., 	Alifax 	Holding 	SpA 	v.
Alcor 	Sci. 	Inc., 	No. 	CV 	14-440 	WES, 	slip 	op. 	at 	19, 	27 	(D.R.I.
Mar. 26, 2019). 	But a Rule 50 analysis is “weighted toward preser-
vation 	of 	the 	jury 	verdict.” 	Rodowicz 	v. 	Massachusetts 	Mut. 	Life
Ins. Co., 279 F.3d 36, 41 (1st Cir. 2002). 	And after scrutinizing
the 	trial 	record, 	the 	Court 	concludes 	that 	there 	was 	a 	legally
sufficient basis to support the jury’s verdict that the Defendants
misappropriated Alifax’s proprietary conversion algorithm.
While 	this 	conclusion 	forecloses 	a 	directed 	verdict 	for 	the
Defendants, 	Alifax’s 	victory 	is 	pyrrhic. 	The 	Court 	finds 	that,
regarding liability, the clear weight of the credible evidence is
17 	See 	Malcolm 	Gladwell, 	Episode 	1: 	Puzzle 	Rush, 	Revisionist
History 	(2019), 	at 	http://revisionisthistory.com/seasons?se-
lected=season-4; Malcolm Gladwell, Episode 2: The Tortoise and the
Hare, 	Revisionist 	History 	(2019), 	at 	http://revisionisthis-
tory.com/seasons?selected=season-4.
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inconsistent with the jury’s verdict; regarding damages, Alifax’s
evidence 	of 	Alcor’s 	gross 	revenues 	allegedly 	attributable 	to 	its
misappropriation 	unfairly 	transgressed 	the 	boundaries 	of 	Rule
1006. 	Thus, a new trial is warranted.
1. 	Legally 	Sufficient 	Evidence 	Supported 	the 	Verdict
that 	Alifax’s 	Conversion 	Algorithm 	Was 	a 	Trade
Secret.
The jury’s finding that the conversion algorithm was a trade
secret was reasonably supported by Alifax’s evidence. 	The “golden
standard” 	for 	determining 	ESR 	is 	known 	as 	the 	Westergren 	test.
See 	Trial 	Tr. 	vol. 	1, 	82:2-5. 	This 	test 	is 	time 	consuming. 	A
technician must mix the blood sample, fill a graduated pipet, wait
an hour while the pipet remains stable, and visually determine the
sedimentation of red blood cells from plasma. 	Id. at 82:15-83:16.
An ESR analyzer automates this process. 	It provides rapid results
by 	taking 	optical 	density 	measurements 	of 	a 	blood 	sample 	in 	just
seconds. 	Id. 	at 	111:8-112:1. 	These 	values 	can 	be 	correlated 	to
the 	results 	from 	hour-long 	Westergren 	tests. 	Id. 	Converting 	the
optical 	data 	into 	a 	reliable, 	Westergren-correlated 	ESR 	value 	is
a critical step in the process. 	See, e.g., id. 94:20-23.
Duic testified that there were “no mathematical models in the
market” for correlating optical signal data to Westergren results
when 	Alifax 	developed 	its 	conversion 	algorithm. 	Id. 	at 	94:2-50.
To 	create 	such 	a 	model, 	Alifax 	ran 	comparative 	tests 	with 	more
than 	40,000 	blood 	samples 	over 	ten 	months. 	Id. 	at 	93:17-21.
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Dr. Enzo Breda (one of Alifax’s co-founders) used these results to
derive 	a 	conversion 	algorithm 	and 	to 	write 	the 	software 	used 	in
Alifax’s 	instruments. 	Id. 	at 	94:2-12; 	Trial 	Tr. 	vol. 	3, 	105:18-
106:4, 	Apr. 	17, 	2019. 	Breda’s 	algorithm 	contained 	four 	easily
identifiable 	numerical 	constants: 	1000, 	3, 	2.2 	and 	1.9. 	Trial
Tr. 	vol. 	3, 	105:24-106:4. 	Without 	a 	correlation 	algorithm, 	Ali-
fax’s 	instruments 	could 	not 	generate 	ESR 	results. 	See 	Trial 	Tr.
vol. 1, 94:20-23; 105:5-17. 	The algorithm was not publicly known
and 	not 	readily 	accessible 	to 	purchasers 	of 	Alifax 	instruments.
See Trial Tr. vol. 3, 96:4-17. 	In addition, as further explained
below, 	at 	least 	one 	rational 	interpretation 	of 	the 	evidence 	sup-
ports 	the 	conclusion 	that 	Alcor 	made 	some 	use 	of 	Alifax’s 	algo-
rithm, 	indicating 	that 	the 	information 	confers 	some 	competitive
advantage. 	This is enough evidence (if barely) to find that Ali-
fax’s conversion algorithm containing four specific constants had
independent economic value from not being generally known or read-
ily ascertainable. 	See R.I. Gen. Laws § 6-41-1.
As 	for 	proof 	that 	Alifax 	undertook 	reasonable 	efforts 	to
maintain 	the 	secrecy 	of 	its 	conversion 	algorithm, 	Duic 	testified
that 	the 	confidentiality 	of 	company 	information 	was 	discussed 	at
development 	meetings 	attended 	by 	Frappa. 	See 	Trial 	Tr. 	vol. 	2,
31:18-32:8; 	Trial 	Ex. 	20. 	Frappa 	attended 	a 	meeting 	at 	Alifax’s
Padova headquarters ten months before his departure where “[c]on-
fidentiality” 	was 	an 	identified 	agenda 	item. 	Trial 	Ex. 	20;
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see also Trial Tr. vol. 2, 32:6-8. 	Alifax provided Frappa with a
company-owned laptop connected to its servers; downloading company
information 	onto 	personal 	devices 	was 	prohibited. 	Id. 	at 	35:2-
24. 	Dr. 	Galiano 	testified 	that 	company 	communications 	were 	con-
sidered 	“confidential.” 	Trial 	Tr. 	vol. 	6, 	98:6-15. 	Emails 	sent
from Alifax accounts had a footer stating that, pursuant to Italian
law, 	the 	email’s 	contents 	were 	“confidential 	and 	intended 	solely
for the use of the individual(s) to whom [the message] is addressed
or otherwise directed.” 	See, e.g., Trial Exs. 20, 34, 36. 	Lastly,
it 	was 	established 	that 	Italy’s 	national 	collective 	bargaining
agreement (“NCBA”) for the mechanical engineering industry imposed
on 	Frappa 	as 	a 	matter 	of 	law 	“a 	post-employment 	duty 	of 	loyalty
prohibiting the disclosure or use of Alifax’s confidential or pro-
prietary information in a manner that was likely to injure Alifax’s
business.” 	See Alifax, 357 F.Supp.3d at 164.
This 	proof 	is 	paper-thin. 	Much 	of 	it 	is 	boilerplate 	stuff,
and there was no evidence showing that Alifax maintains or enforces
any 	written 	policies, 	procedures, 	or 	protocols 	touching 	on 	the
confidentiality 	of 	its 	information. 	There 	was 	no 	evidence 	that
Alifax 	ensured 	that 	Frappa 	(or 	any 	similarly 	situated 	employee)
knew and understood the terms of the NCBA. 	It is frankly stunning
to find that an international medical instrument company may rely
largely 	on 	the 	wording 	of 	a 	generic 	email 	footer 	to 	ensure 	the
confidentiality 	of 	its 	sensitive 	communications. 	Nevertheless,
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Rule 50 does not require a party to weld an air-tight case. 	When
viewed 	in 	the 	light 	most 	favorable 	to 	the 	verdict, 	this 	evidence
was sufficient to support the jury’s conclusion that Alifax’s took
reasonable efforts under the circumstances to maintain the secrecy
of its conversion algorithm. 	Accordingly, there was enough proof
to support the jury’s verdict that the algorithm comprised a trade
secret and to preclude judgment as a matter of law for the Defend-
ants. 	See R.I. Gen. Laws § 6-41-1.
2. 	Legally 	Sufficient 	Evidence 	Supported 	the 	Verdict
that 	the 	Defendants 	Willfully 	Misappropriated
Alifax’s Conversion Algorithm.
An 	accusation 	of 	theft 	lies 	at 	the 	heart 	of 	this 	dispute:
Alifax’s 	claim 	that 	the 	Defendants 	willfully 	misappropriated 	its
secret 	formula 	for 	obtaining 	ESR 	values. 	At 	trial, 	the 	parties’
set out conflicting narratives about how Alcor developed the iSED.
Rule 	50 	does 	not 	permit 	the 	Court 	to 	decide 	who 	was 	the 	more
persuasive 	storyteller. 	What 	matters 	is 	whether 	the 	trial 	evi-
dence, 	when 	considered 	in 	the 	most 	flattering 	light, 	reasonably
supports Alifax’s rendition.
According to Alifax, Frappa had access to the company’s con-
fidential 	information, 	including 	its 	source 	code 	and 	proprietary
conversion 	algorithm. 	Trial 	Tr. 	vol. 	2, 	19:13-20, 	22:15-23:10;
Trial 	Exs. 	9, 	11. 	In 	August 	2011, 	Frappa 	met 	with 	Alcor’s 	CEO,
Carlo 	Ruggeri, 	in 	Rhode 	Island 	and 	discussed 	whether 	they 	might
work 	together 	on 	an 	ESR-related 	project. 	Ruggeri 	Dep.
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82:12-83:23, 	90:1-25.18 	He 	departed 	Alifax 	two 	months 	later 	and
began 	working 	with 	Alcor 	almost 	immediately. 	See 	Trial 	Exs. 	28,
39, 40.
Alcor 	had 	attempted 	to 	develop 	its 	own 	ESR 	analyzer 	with 	an
Italian company, Hospitex, in 2010. 	See Trial Ex. 21. 	That effort
was 	unsuccessful, 	but 	a 	changing 	tide 	accompanied 	Frappa’s 	arri-
val. 	Within eight months of Frappa joining the team, Alcor debuted
a 	new 	instrument 	at 	the 	June 	2012 	trade 	show 	for 	the 	American
Association for Clinical Chemistry (“AACC”): the iSED. 	See Ruggeri
Dep. 143:7-144:11; Trial Tr. vol. 5, 51:18-20; Trial Ex. 77.
Marketing 	materials 	announced 	that 	the 	instrument 	wasn’t
“from 	the 	future” 	but 	rather 	“here 	and 	now,” 	touting 	the 	iSED’s
ability to achieve results in twenty seconds with “walk away pro-
cessing” 	capabilities. 	Trial 	Ex. 	77. 	Alcor 	beckoned 	potential
customers 	to 	have 	a 	look 	– 	“Seeing 	is 	believing.” 	Id. 	An 	August
6, 	2012 	internal 	Alcor 	email 	authored 	by 	its 	marketing 	director,
Mark 	Ecker, 	states 	that 	the 	company 	“has 	a 	fully 	functional 	pro-
totype for everyone to see and review.” 	Trial Ex. 82.
Several months later, on November 6, 2012, Frappa “committed”
iSED 	software 	source 	code 	titled 	“RECHON.C” 	to 	Alcor’s 	Bitbucket
repository. 	Trial 	Tr. 	vol. 	5, 	38:3-40:10; 	Trial 	Ex. 	65. 	Source
18 	Alifax 	played 	Carlo 	Ruggeri’s 	deposition 	in 	part 	as 	part
of its case-in-chief. 	See Fed. R. Civ. P. 32(a)(3).
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code is comprised of commands written in a human-readable computer
programming 	language. 	Bitbucket 	is 	the 	brand 	name 	of 	Alcor’s
source 	code 	version 	control 	repository. 	See 	Trial 	Tr. 	vol 	3,
126:15-17; 128:6-7. 	Bitbucket shows when a user adds, deletes, or
alters 	code; 	it 	tracks 	historical 	revisions 	in 	much 	the 	same 	way
an 	author 	might 	keep 	an 	electronic 	file 	of 	redlined 	manuscript
drafts. 	Id. at 126:21-23. 	A change to the source code is called
a 	“commit” 	and 	reflects 	a 	snapshot 	of 	the 	code 	as 	of 	a 	certain
date. 	Id. at 127:14-17.
The November 6 commit identified Frappa as its author and was
titled 	“Version 	1.00A.” 	See 	Trial 	Tr. 	vol. 	5, 	41:5-7; 	Trial 	Ex.
65. 	On its face, the code appears to contain the numbers 1000, 3,
2.2 and 1.9.19 	Trial Ex. 65, 3-4. 	Alifax also introduced evidence
of 	a 	second 	source 	code 	file. 	See 	Trial 	Ex. 	156; 	Trial 	Tr. 	vol.
3, 	106:9-25. 	This 	code 	was 	not 	from 	a 	Bitbucket 	commit; 	it 	is
code produced by Alcor outside the Bitbucket environment in a file
folder 	with 	the 	title 	“1.04A.” 	See 	id.; 	Trial 	Tr. 	vol. 	3, 	128:6-
22; 	Trial 	Tr. 	vol. 	4, 	18:6-16, 	Apr. 	18, 	2019. 	Alifax’s 	expert,
19 	Alcor 	cites 	the 	testimony 	of 	Alcor’s 	Chief 	Technology 	Of-
ficer, 	Peter 	Sacchetti, 	as 	additional 	support 	for 	this 	proposi-
tion. 	Sacchetti 	denied 	recognizing 	any 	conversion 	constants 	or
algorithm in in Exhibit 65 at trial. 	Alifax’s counsel repeatedly
confronted 	Sacchetti 	with 	prior 	inconsistent 	statements 	from 	his
deposition, 	but 	such 	statements 	were 	admissible 	only 	to 	impeach
Sacchetti’s 	credibility; 	they 	could 	not 	be 	considered 	for 	their
truth. 	See 	United 	States 	v. 	Hudson, 	970 	F.2d 	948, 	956 	(1st 	Cir.
1992).
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Dr. Bryan Bergeron, explained that the 1.04A file contained “math
source 	code” 	for 	the 	iSED 	and 	identified 	Alifax’s 	conversion 	al-
gorithm (with its four constants) in that code. 	Trial Tr. vol. 3,
106:9-107:19. 	See also Trial Ex. 156 at ALCOR-0092342. 	He could
not, 	however, 	pinpoint 	when 	the 	code 	contained 	in 	the 	1.04A 	file
was written or used because he never compared it to the historical
Bitbucket record. 	Trial Tr. vol. 4, 21:5-14.
Several weeks after the November 6 commit, Frappa drafted an
“iSED® 	Automated 	ESR 	Analyzer 	Correlation 	Test 	Protocol.” 	Trial
Ex. 	92; 	Frappa 	Dep. 	54:24-55:10. 	Frappa’s 	protocol 	is 	dated 	No-
vember 29, 2012 and provides the specific steps for a correlation
study designed to compare ESR values obtained from an iSED to those
obtained from the Westergren method. 	Trial Ex. 92. 	The protocol
specifically 	instructs 	that 	all 	instrument 	printouts 	should 	be
saved 	and 	that 	results 	should 	be 	recorded 	on 	both 	handwritten
charts 	and 	an 	Excel 	spreadsheet. 	Id. 	at 	3. 	It also 	states 	that
tests should be carried out with an iSED running “software version
1.00.” 	Id. at 1.
Frappa 	made 	a 	“[f]irst 	commit” 	of 	the 	iSED 	“MATH.c” 	source
code file to Bitbucket on December 1, 2012. 	Trial Ex. 470. 	Alcor
began correlation testing using blood samples from Rhode Island’s
Fatima 	Hospital 	in 	late 	January 	2013 	to 	develop 	a 	conversion 	al-
gorithm. 	See 	Trial 	Tr. 	vol. 	5, 	68:13-69:3, 	70:8-73:14, 	Apr. 	22,
2019; 	Trial 	Exs. 	95, 	97, 	98. 	Frappa 	began 	revising 	the 	MATH.c
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source code following these tests on January 28, 2013. 	Trial Ex.
470. 	Alcor 	refined 	its 	conversion 	algorithm 	over 	the 	ensuing
months. 	It 	performed 	additional 	correlation 	testing 	in 	partner-
ship 	with 	Rhode 	Island 	Hospital 	in 	June 	2013. 	See 	Trial 	Tr. 	vol
5, 	73:21-74:13; 	Trial 	Exs. 	93, 	104, 	197. 	The 	outcome 	of 	this
process 	was 	a 	fourth-degree 	polynomial 	equation. 	See 	Trial 	Tr.
vol. 5, 82:8-83:2; Trial Exs. 104, 122; see also Trial Tr. vol. 8,
44:3-22, 	April 	26, 	2019. 	This 	equation 	comprises 	the 	conversion
algorithm 	Alcor 	uses 	in 	its 	iSED 	instruments. 	Trial 	Tr. 	vol. 	6,
16:12-22.
Alifax does not dispute that the Defendants developed a com-
plex equation through correlative testing between late January and
June 2013. 	It claims instead that the Defendants ran other tests
between December 21, 2012 and January 9, 2013 with a device using
its proprietary algorithm (not an equation developed from testing
at Fatima and Rhode Island Hospital), achieved better results, and
exploited its use of the algorithm to market its instrument. 	This
theory requires a detailed unpacking.
Trial 	Exhibit 	92 	is 	the 	cornerstone 	of 	Alifax’s 	argument.
Attached to Frappa’s protocol are results from a “Correlation Study
for 	ESR 	– 	ISED 	vs. 	CLSI 	ESR.”20 	This 	section 	of 	the 	exhibit 	is
20 	CLSI 	ESR 	is 	a 	reference 	to 	the 	“approved 	standard 	method-
ology (Westergren).” Trial Ex. 92.
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written 	in 	a 	different 	font 	and 	style 	from 	the 	protocol 	but 	is
consecutively Bates-numbered. 	The correlation study was conducted
with 	“300 	samples 	from 	healthy 	subjects” 	and 	includes 	a 	set 	of
typewritten 	and 	handwritten 	worksheets 	with 	the 	same 	data. 	Id.
The 	worksheets 	record 	ESR 	results 	for 	311 	samples 	using 	both 	the
Westergren method and the iSED. 	Id. 	Each worksheet is signed by
Frappa and has one of five handwritten dates: 	12/21/12, 12/24/12,
1/03/13, 	1/08/13 	and 	1/09/13. 	Id. 	at 	5-24. 	Consistent 	with 	the
protocol, 	the 	last 	pages 	of 	Trial 	Exhibit 	92 	contain 	printouts
from 	an 	iSED. 	Id. 	at 	25-31. 	The 	printouts 	identify 	the 	test
instrument as number “00027” and have a filename that corresponds
to a date, e.g., “File: 122112.XML.” 	Id. at 25. 	The handwritten
date on each page matches the instrument-generated date. 	Id. 	The
second 	page 	of 	the 	attachment 	reports 	a 	correlation 	of 	“0.9569”
between the iSED results and the Westergren tests. 	Id. at 2. 	(The
Court refers to these results hereafter as the “Disputed Correla-
tion Tests.”)
Alifax offered Frappa’s deposition testimony about Trial Ex-
hibit 92 during its case-in-chief. 	Frappa confirmed that the dates
and 	signatures 	on 	the 	ESR 	worksheets 	were 	in 	his 	handwriting.
Frappa Dep. 56:12-57:1. 	He confirmed that the printouts were from
a prototype iSED and that the filenames correspond to the date the
file was created. 	Id. at 57:11-13, 58:1-8, 63:25-64:6. 	He agreed
that, 	based 	on 	the 	additional 	handwritten 	dates, 	the 	tests 	were
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performed 	on 	the 	dates 	indicated. 	Id. 	at 	58:21-21. 	He 	further
agreed 	that 	a 	prototype 	instrument 	obtained 	actual 	ESR 	results
from 	the 	blood 	samples. 	Id. 	at 	59:22-60:3. 	In 	other 	words, 	the
instrument obtained more than the raw optical measurements or the
sample 	aggregation 	index21; 	it 	was 	performing 	a 	conversion. 	He
could 	not 	recall 	the 	algorithm 	that 	the 	prototype 	used. 	Id. 	at
65:12-19.
Both 	Trial 	Exhibit 	92 	and 	the 	Rhode 	Island 	Hospital 	Report
include 	scatter 	plots 	depicting 	the 	fit 	among 	the 	iSED-obtained
ESR 	values 	and 	those 	from 	the 	Westergren 	tests. 	See 	Trial 	Exs.
92, 	197. 	Trial 	Exhibit 	92 	expressly 	states 	that 	nearly 	a 	96%
correlation exists between the two values. 	See Trial Ex. 92 at 2.
The Rhode Island Hospital Report does not provide such a calcula-
tion 	(known 	as 	an 	r-squared 	value). 	Regardless, 	a 	side-by-side
comparison22 of 	the 	two 	scatter 	plots 	(both 	contained 	in 	admitted
exhibits) 	reveals 	that 	the 	Disputed 	Correlation 	Tests 	appear 	to
have a higher correlation:
21 	For 	a 	more 	detailed 	explanation 	of 	how 	the 	device 	works,
see 	Alifax Holding SpA v. Alcor Sci. Inc, No. CV 14-440 WES, slip
op. at 4-5 (D.R.I. Mar. 26, 2019).
22 Alifax elicited testimony at trial concerning how a scatter
plot 	demonstrates 	the 	strength 	of 	a 	correlation. 	See 	Trial 	Tr.
vol. 5, 64:6-65:4, April 25, 2019. 	In layman’s terms, the stronger
the 	correlation, 	the 	closer 	the 	plotted 	data 	cluster 	to 	the 	line
depicted on the graph. 	See id.
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TRIAL EXHIBIT 9223 	TRIAL EXHIBIT 197
According 	to 	Alcor’s 	Chief 	Technology 	Officer, 	Peter 	Sacchetti,
the 	data 	in 	Trial 	Exhibit 	92 	were 	submitted 	to 	the 	U.S. 	Food 	and
Drug 	Administration 	by 	Alcor 	to 	support 	a 	2014 	application 	made
under the Clinical Laboratory Improvement Amendments, 42 U.S.C. §
263a (“CLIA”).24 	Trial Tr. vol. 5, 93:25-94:8; Trial Ex. 116. 	The
data was used to respond to the application reviewer’s request for
the 	comparison 	studies 	verifying 	Alcor’s 	claim 	that 	the 	iSED
23 	Trial 	Exhibit 	92 	contains 	two 	scatter 	plots 	that 	are 	sub-
stantially 	similar. 	The 	graph 	depicted 	here 	limits 	the 	range 	to
15 to 105 mm/h, whereas the other graph plots all data.
24 There was unrebutted evidence that government clearance was
not necessary to sell the iSED. See, e.g., Trial Tr. vol. 6, 33:3-
10; Trial Tr. vol. 7, 12:22-24, 13:12-15; Trial Ex. 94. 	The CLIA
classification 	level 	(e.g., 	“moderately 	complex” 	or 	“highly 	com-
plex”) 	merely 	governs 	how 	a 	purchasing 	laboratory 	operates 	the
instrument in question. 	Trial Tr. vol. 6, 33:3-10.
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produces 	twenty-second 	ESR 	results 	correlated 	to 	Westergren 	val-
ues. 	See Trial Ex. 114 at ALCOR-0072693.
Alifax 	constructs 	the 	following 	argument 	to 	show 	misappro-
priation by improper use based on this evidence:
• 	Trial Exhibit 92 shows that Alcor had a functioning
prototype 	iSED 	no 	later 	than 	December 	21, 	2012.
Frappa’s 	protocol 	called 	for 	the 	use 	of 	an 	iSED,
and whatever prototype he used to conduct the Dis-
puted 	Correlation 	Tests 	generated 	actual 	ESR 	re-
sults 	with 	a 	96% 	correlation 	to 	the 	industry
standard Westergren method.
• 	Alcor did not begin writing its own conversion al-
gorithm 	until 	January 	28, 	2013. 	If 	a 	prototype
iSED was obtaining ESR values before that date, it
must 	have 	been 	using 	some 	other 	conversion 	algo-
rithm.
• 	Frappa 	knew 	Alifax’s 	conversion 	algorithm 	and 	in-
corporated 	it 	into 	Alcor 	code 	for 	some 	purpose
prior 	to 	December 	21, 	2012. 	This 	is 	supported 	by
evidence 	that 	versions 	1.00A 	and 	1.04A 	of 	Alcor’s
source 	code 	(at 	least 	one 	of 	which 	predates 	the
Disputed Correlation Tests) contained Alifax’s con-
version algorithm and constants.
The 	jury 	could 	have 	made 	several 	reasonable 	inferences 	from 	this
evidence. 	First, because Alifax’s algorithm was the only algorithm
Alcor 	had 	before 	January 	28, 	2012, 	the 	Defendants 	must 	have 	used
it to obtain results from the iSED during the Disputed Correlation
Tests. 	Alifax argued that Alcor submitted the Disputed Correlation
Tests 	to 	support 	its 	2014 	CLIA 	application 	because 	they 	appeared
to 	have 	a 	stronger 	correlation 	to 	the 	Westergren 	method 	than 	the
June 2013 Rhode Island Hospital tests. 	Furthermore, Alifax argues
that (by working backwards from December 2012) the jury could infer
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that 	Alcor 	could 	only 	have 	made 	its 	marketing 	claims 	at 	the 	2012
AACC 	trade 	show 	as 	well 	as 	in 	its 	August 	6, 	2012 	email 	(the 	gist
of which was that the company presently had a functioning instru-
ment) if it was already using Alifax’s proprietary information.25
These arguments are circumstantial to be sure. 	That alone is
unremarkable. 	See, e.g., Pioneer Hi-Bred Int’l. v. Holden Found.
Seeds, 	Inc., 	35 	F.3d 	1226, 	1239 	(8th 	Cir.1994) 	(“Wrongful 	taking
of a trade secret can be found based on circumstantial evidence.”
(quoting 	Roger M. Milgrim, Trade Secrets § 15.01[1], at 15–18 n.
10 	(1993) 	(collecting 	cases)); 	RKI, 	Inc. 	v. 	Grimes, 	177 	F. 	Supp.
2d 	859, 	876 	(N.D. 	Ill. 	2001) 	(“Because 	direct evidence of 	theft
and use of trade secrets is often not available, the plaintiff can
rely 	on circumstantial evidence to 	prove misappropriation by
drawing inferences from 	perhaps 	ambiguous circumstantial evi-
dence.”). 	The evidence confirms Alifax’s story, however, only if
it 	receives 	the 	benefit 	of 	every 	reasonable 	inference. 	Rule 	50
requires 	such 	indulgences. 	The 	Court 	therefore 	agrees 	that 	the
jury’s misappropriation verdict is supported by a rational inter-
pretation of Alifax’s evidence. 	See Astro-Med, 591 F.3d at 18-19
(affirming denial of Rule 50 motion as, among other reasons, there
“is a logical inference that a competitor who hires away a rival’s
25 	This 	latter 	argument 	was 	plainly 	the 	basis 	for 	the 	jury’s
award of damages on Count II, the propriety of which is discussed
further below.
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valued 	employee 	with 	access 	to 	inside 	information 	has 	done 	so 	in
order 	to 	use 	that 	inside 	information 	to 	compete 	with 	the 	rival 	.
. 	. 	”); 	GlobeRanger 	Corp. 	v. 	Software 	AG 	USA, 	Inc.,
No. 3:11-CV-0403-B, 2015 WL 3648577, *13 (N.D. Tex. June 11, 2015)
(denying 	Rule 	50 	motion 	as 	evidence 	showed 	defendant 	“relied 	on
[plaintiff’s 	technology] 	to 	develop 	its 	own.” 	(citing 	Wellogix,
Inc. 	v. 	Accenture, 	L.L.P., 	716 	F.3d 	867, 	877 	(5th 	Cir. 	2013)
(denying 	judgment 	as 	a 	matter 	of 	law 	where 	documents 	suggested
defendants 	had 	access 	to 	plaintiff’s 	source 	code 	and 	were 	using
its content)).
The Defendants focus tightly on the lack of evidence showing
Alcor 	sold 	any 	device 	containing 	Alifax’s 	conversion 	algorithm.
See 	Renewed 	Mot. 	for 	JMOL 	at 	23. 	Without 	a 	doubt, 	Alifax 	at 	one
time focused its attention on the use of its conversion algorithm
in 	production 	instruments 	sold 	to 	customers. 	See, 	e.g., 	Pl.’s
Mem. of Law in Opp’n to Defs.’ Mot. for Partial Summary J. 20-21,
ECF 	No. 	161-1. 	And 	as 	discussed 	throughout 	this 	opinion, 	it 	is
also undeniable that Alifax’s liability theories morphed through-
out 	this 	litigation, 	including 	mid-trial. 	But 	as 	the 	foregoing
summary 	shows, 	there 	is 	some 	proof 	that 	– 	if 	believed 	– 	supports
finding 	that 	the 	Defendants 	had 	something 	more 	than 	a 	“dead 	end
flirtation” 	with 	Alifax’s 	confidential 	information. 	On-Line
Techs., 	Inc. 	v. 	Perkin-Elmer 	Corp., 	253 	F.Supp.2d 	313, 	332 	(D.
Conn. 2003). 	To conclude otherwise, the Court would have to weigh
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the 	evidence 	and 	reject 	Alifax’s 	(and 	presumably 	the 	jury’s) 	in-
terpretation of Trial Exhibit 92 (which Alifax bolstered at trial
with 	Frappa’s 	own 	deposition) 	as 	well 	as 	Alcor’s 	June 	and 	August
2012 	statements. 	Rule 	50’s 	strict 	requirements 	prohibit 	this.
Judgment 	as 	a 	matter 	of 	law 	on 	the 	issue 	of 	misappropriation 	of
the algorithm is therefore inappropriate.
3. 	Legally 	Sufficient 	Evidence 	Supported 	The 	Jury’s
Award of “Head Start” Damages.
Alifax presented the jury with two alternative approaches for
calculating 	unjust 	enrichment 	damages: 	(1) 	one 	year 	of 	profits
reflecting 	the 	unfair 	head 	start 	Alcor 	obtained 	by 	launching 	the
iSED 	at 	the 	2012 	AACC; 	or 	(2) 	the 	financial 	benefit 	Alcor 	has
obtained 	from 	the 	iSED’s 	“moderately 	complex” 	CLIA 	designation,
which 	was 	supported 	in 	part 	by 	the 	Disputed 	Correlation 	Tests.
See 	Trial 	Tr. 	vol. 	12, 	47:24-48:5, 	49:18-21, 	51:9-53:10, 	55:4-9,
May 	2, 	2019. 	The 	jury 	awarded 	Alifax 	$6.5 	million 	dollars. 	Jury
Verdict: Phase II: Damages, ECF No. 299.
First, 	a 	procedural 	point. 	Alcor 	adequately 	preserved 	its
Rule 	50 	arguments 	that 	Alifax’s 	damages 	methodologies 	were 	not
causally 	connected 	to 	misappropriation 	of 	the 	conversion 	algo-
rithm. 	A party may only raise grounds under Rule 50(b) (a renewed
motion 	for 	judgment 	as 	a 	matter 	of 	law) 	that 	it 	preserved 	in 	a
Rule 50(a) motion at the close of the evidence. 	Parker v. Gerrish,
547 	F.3d 	1, 	12 	(1st 	Cir. 	2008). 	Rule 	50(a) 	does 	not, 	however,
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require a party to detail its reasoning with “technical precision”
mid-trial. 	Lynch v. City of Boston, 180 F.3d 1, 13 n.9 (1st Cir.
1999). 	All the rule requires is reasonable notice of the party’s
legal position. 	Id. (stating reasons should be stated “with suf-
ficient certainty to apprise the court and opposing counsel of the
movant’s position with respect to the motion.”); see also Western
Union 	Co. 	v. 	MoneyGram 	Payment 	Sys., 	Inc., 	626 	F.3d 	1361, 	1367
(Fed. Cir. 	2010)(“[E]ven a cursory motion suffices . . . so long
as it ‘serves the purposes of Rule 50(a), i.e., to alert the court
to 	the 	party's 	legal 	position 	and 	to 	put 	the 	opposing 	party 	on
notice 	of 	the 	moving 	party's 	position 	as 	to 	the 	insufficiency 	of
the 	evidence.’”) 	quoting 	Blackboard, 	Inc. 	v. 	Desire2Learn, 	Inc.,
574 F.3d 1371, 1379-1380 (Fed. Cir. 2009)).
The 	First 	Circuit’s 	holding 	in 	Osorio 	v. 	One 	World 	Techs.,
Inc., 	659 	F.3d 	81 	(1st 	Cir. 	2011), 	is 	an 	apt 	analog. 	In 	this
product 	liability 	action, 	Osorio 	argued 	that 	defendant 	Ryobi’s
bench top table saw was unacceptably dangerous due to a defective
design. 	Id. at 83. 	In its Rule 50(a) motion, Ryobi argued Osorio
“failed 	to 	offer 	sufficient 	evidence 	. 	. 	. 	that 	the 	subject 	saw
was 	not 	designed 	with 	reasonable 	care 	or 	that 	the 	saw 	was 	both
defective 	and 	unreasonable 	dangerous.” 	Id. 	at 	87-8. 	In 	its 	re-
newed motion under Rule 50(b), Ryobi not only doubled down on its
sufficiency 	attack, 	but 	also 	argued 	that 	Osorio’s 	expert 	witness
impermissibly 	advanced 	a 	“categorical 	liability” 	argument 	that
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suggested 	all 	“low-cost 	portable 	benchtop 	table 	saws” 	were 	“in-
herently unsafe.” 	Id. at 87. 	Osorio argued on appeal that Ryobi
had waived its argument regarding categorical liability.
The 	First 	Circuit 	disagreed. 	Ryobi’s 	objection 	to 	the 	ex-
pert’s 	testimony 	was 	a 	“corollary 	to 	[Ryobi’s] 	sufficiency 	argu-
ment” 	that 	“flesh[ed] 	out” 	the 	question 	of 	whether 	the 	plaintiff
satisfied his burden of proof - an issue the court noted that Ryobi
had contested at each stage of the litigation.” Id. at 88. 	Alcor,
like 	Ryobi, 	made 	a 	distinct 	insufficiency 	argument 	in 	its 	Rule
50(a) motion: “Alifax did not satisfy its burden of proving Alcor’s
gross 	sales 	attributable 	to 	the 	misappropriation 	. 	. 	. 	Alifax
presented no evidence that [Alcor’s gross sales] are attributable
to the misappropriated computer code trade secret. 	Demonstrating
Alcor’s 	general 	gross 	sales 	is 	not 	sufficient.” 	Trial 	Tr. 	vol.
12, 	10:7-20. 	Thus, 	as 	in 	Osorio, 	Alcor’s 	specific 	objections 	to
Alifax’s 	CLIA 	designation 	and 	head-start 	calculations 	simply
“flesh out” an insufficiency argument that Alcor pressed at every
stage of this litigation. 	There was no waiver.26
26 	Even 	if 	the 	Court 	had 	found 	that 	these 	objections 	were
waived, 	it 	would 	nevertheless 	have 	granted 	a 	new 	trial. 	See 	9B
Charles Alan Wright & Arthur R. Miller, Federal Practice and Pro-
cedure § 2537 (3d ed. 2008).
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Now to the meat of the issue. 	A plaintiff may recover under
RIUTSA 	“both 	the 	actual 	loss 	caused 	by 	misappropriation 	and 	the
unjust 	enrichment 	caused 	by 	misappropriation 	that 	is 	not 	taken
into account in computing actual loss.” 	R.I. Gen. Laws 6-41-3(a).
“In 	lieu 	of 	damages 	measured 	by 	any 	other 	methods, 	the 	damages
caused 	by 	misappropriation 	may 	be 	measured 	by 	imposition 	of 	lia-
bility for a reasonable royalty for a misappropriator’s unauthor-
ized disclosure or use of a trade secret.” 	Id. 	A jury’s damages
award need only reflect a reasonable estimate based on a rational
model. 	Abbey 	Med./Abbey 	Rents, 	Inc. 	v. 	Mignacca, 	471 	A.2d 	189,
195 (R.I. 1984).
Here, 	Alifax 	sought 	only 	unjust 	enrichment 	damages. 	After
hearing truncated arguments mid-trial, the Court adopted the bur-
den-shifting 	framework 	set 	forth 	in 	the 	Restatement 	(Third) 	of
Unfair Competition with respect to this theory.27 	The Restatement
provides:
The 	general 	rules 	governing 	accountings 	of
profits 	are 	applicable 	in 	trade 	secret 	ac-
tions. 	The 	plaintiff 	is 	entitled 	to 	recover
the defendant's net profits. The plaintiff has
the 	burden 	of 	establishing 	the 	defendant’s
sales; the defendant has the burden of estab-
lishing any portion of the sales not attribut-
able 	to 	the 	trade 	secret 	and 	any 	expenses 	to
be deducted in determining net profits.
27 	The 	Court 	made 	it 	abundantly 	clear 	to 	the 	parties 	that
their dispute over whether to apply the Restatement’s burden shift-
ing 	framework 	was 	brought 	to 	the 	Court’s 	attention 	at 	the 	last
possible moment with unsatisfactory briefing and argument.
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Restatement (Third): Unfair Competition § 45, cmt. f (Am. Law Inst.
2019). 	Nothing 	in 	the 	Restatement’s 	framework 	relieved 	Alifax
from its obligation to prove causation in the first instance. 	Id.
(“The 	traditional 	form 	of 	restitutionary 	relief 	in 	an 	action 	for
the 	appropriation 	of 	a 	trade 	secret 	is 	an 	accounting 	of 	the 	de-
fendant’s 	profits 	on 	sales 	attributable 	to 	the 	use 	of 	the 	trade
secret.”) 	(emphasis 	added); 	see 	also 	id. 	cmt. 	b. 	(“The 	plaintiff
bears 	the 	burden 	of 	proving 	the 	fact 	and 	cause 	of 	any 	loss 	for
which recovery is sought.”); R.I. 	Gen. Laws § 6-41-3(a) (“Damages
can 	include 	. 	. 	. 	the 	unjust 	enrichment 	caused 	by 	misappropria-
tion”). 	The 	Court 	instructed 	the 	jury 	suitably. 	See 	Jury 	In-
structions: Phase II: Damages 8-9, ECF No. 298.28
The evidence supporting Alifax’s argument that Alcor unjustly
benefited from the iSED’s CLIA designation was inadequate. 	Alifax
presented practically no evidence about the CLIA designation pro-
cess. 	Although 	it 	claims 	that 	Alcor 	obtained 	a 	“moderately 	com-
plex” designation for the iSED, Alifax introduced almost no proof
of 	that 	fact 	– 	no 	public 	records, 	no 	device 	specifications, 	no
28 	The 	Court 	instructed: 	“If 	you 	find 	that 	Alifax 	has 	proven
that 	Alcor 	benefitted 	from 	using 	the 	computer 	code 	trade 	secret,
you 	may 	award 	the 	monetary 	value 	you 	find 	has 	been 	proven 	by 	a
preponderance of the evidence to be attributable to that benefit.”
Id. at 8. 	It also instructed: “Alifax must prove by a preponder-
ance of the evidence Alcor’s gross sales attributable to its mis-
appropriation 	of 	the 	computer 	code 	trade 	secret.” 	Id. 	at 	9
(emphasis added).
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testimony. 	Its best evidence was a statement in an undated draft
iSED 	operator’s 	manual. 	See 	Trial 	Exhibit 	460. 	Even 	assuming
this 	meagre 	statement 	sufficed, 	there 	was 	no 	evidence 	that 	FDA
clearance 	or 	a 	particular 	CLIA 	designation 	was 	necessary 	to 	sell
iSED instruments. 	Indeed, the record from Alifax’s case-in-chief
is 	at 	odds 	with 	its 	own 	position. 	See, 	e.g., 	Trial 	Tr. 	vol. 	6,
33:3-10; Trial Ex. 94.
The 	strongest 	nail 	in 	the 	CLIA-based 	calculation 	coffin 	is
the complete dearth of evidence about why customers purchased the
iSED. 	Alifax offered no proof that a moderately complex designa-
tion 	drove 	sales 	in 	the 	clinical 	instrument 	industry. 	There 	was
no 	evidence 	that 	a 	“moderately 	complex” 	designation 	led 	to 	even
one sale of an iSED.29 	One statement from Ruggeri that one customer
asked about the iSED’s designation cannot sustain an inference of
causation. 	See 	Trial 	Ex. 	114 	at 	ALCOR-0072694. 	It 	follows 	that
any 	calculation 	of 	damages 	based 	on 	the 	iSED’s 	purported 	CLIA
designation 	would 	have 	been 	pure 	speculation 	on 	the 	part 	of 	the
jury. 	See McLaughlin v. Moura, 754 A.2d 95, 98 (R.I. 2000)(holding
that the causal connection between plaintiff’s cause of action and
damages “may not be based on conjecture or speculation”).
29 If anything, the evidence was to the contrary. 	For example,
Ecker boasted about an “incredible” response from customers at the
2012 AACC trade show, which was two years before the iSED applied
for a CLIA designation. 	See Trial Ex. 78.
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But 	this 	conclusion 	does 	not 	end 	the 	Court’s 	inquiry. 	If 	a
party presents multiple damages calculations, an award may survive
so long at least one of the alternatives has a sufficient eviden-
tiary 	foundation. 	See 	Northpoint 	Tech., 	Ltd. 	v. 	MDS 	Am., 	Inc.,
413 	F.3d 	1301, 	1312 	(Fed. 	Cir. 	2005) 	(“[W]here 	there 	are 	two 	al-
ternative 	factual 	theories 	which 	might 	support 	the 	verdict, 	the
verdict will be upheld if there is sufficient evidence to support
either theory[.]”) quoting Baumler v. State Farm Mut. Auto. Ins.,
493 	F.2d 	130, 	134 	(9th 	Cir.1974)); 	Bank 	of 	Am. 	Nat’l 	Trust 	&
Savings 	Ass’n 	v. 	Hayden, 231 	F.2d 	595, 	602–03 	(9th 	Cir.
1956) (holding where the parties present alternative damages cal-
culations, 	the 	verdict 	should 	be 	upheld 	if 	there 	is 	sufficient
evidence 	in 	the 	record 	as 	to 	any 	calculation). 	The 	Court 	must
therefore 	consider 	whether 	the 	evidence 	supports 	the 	proffered
head start computation.
Alifax 	introduced 	evidence 	that 	the 	AACC 	trade 	show 	was 	a
lucrative venue for launching new products, particularly diagnos-
tic 	instruments 	like 	the 	iSED. 	See 	Trial 	Tr. 	vol. 	6, 	69:4-17.
Ruggeri conceded that Alcor needed “to meet the deadline of having
a working prototype” for this event. 	Ruggeri Dep. 135:8-13. 	“Time
was 	[of] 	the 	essence,” 	he 	said. 	Id. 	at 	135:7-9. 	Frappa 	shared
Ruggeri’s 	concern. 	Just 	weeks 	before 	the 	show, 	he 	wrote 	to 	a
collaborator 	about 	the 	time 	required 	to 	finish 	a 	circuit 	board
component, 	explaining 	that 	“the 	project 	is 	very 	important” 	and
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that “even a little delay should be a big problem. 	We cannot miss
this 	deadline.” 	Trial 	Ex. 	67. 	As 	explained 	above, 	there 	was 	at
least some evidence that Alcor succeed in creating a “fully func-
tioning 	prototype” 	used 	to 	market 	the 	iSED 	by 	misappropriating
Alifax’s conversion algorithm.
Dr. 	Bergeron 	described 	the 	task 	of 	developing 	a 	conversion
algorithm 	as 	a 	“hard 	problem” 	that 	would 	require 	a 	prototype 	in-
strument 	and 	“many 	experiments[] 	to 	collect 	data.”30 	Trial 	Tr.
vol. 	3, 	115:16-17, 	116:3. 	He 	opined 	that 	it 	would 	“definitely
take 	months” 	for 	Alcor 	to 	develop 	its 	own 	commercially 	viable
algorithm. 	Id. 	117:23-116:1. 	Alcor’s 	development 	timeline 	for
30 	As 	the 	Court 	observed 	in 	its 	order 	excluding 	the 	trade
secret 	misappropriation 	damages 	opinion 	of 	Christopher 	Bokhart,
Dr. Bergeron’s did not disclose an opinion that developing a con-
version algorithm would take “months” in his report. Alifax Holding
SpA v. Alcor Sci. Inc., 2019 WL 1930763, *4 n.11 (Apr. 30, 2019).
The Court made its observation sua sponte. Alcor did not object to
that testimony at trial; it chose to cross-examine Dr. Bergeron on
his 	statement 	instead. 	Trial 	Tr. 	vol. 	3, 	115:23-116:9, 	119:10-
120:6. 	Indeed, 	Alcor 	has 	never 	moved 	to 	strike 	Dr. 	Bergeron’s
questionable testimony. 	The proper avenue to challenge this evi-
dence would have been a contemporaneous trial objection, not post-
trial 	briefing. 	See 	Fed. 	R. 	Evid. 	103; 	Waitek 	v. 	Dalkon 	Shield
Claimants 	Tr., 	934 	F. 	Supp. 	1068, 	1083 	(N.D. 	Iowa 	1996) 	(“[T]he
trial court is not ‘required to exercise its gatekeeping authority
over expert testimony without 	an 	objection’”), aff’d, 114 	F.3d
117 (8th Cir. 1997) (quoting McKnight By & Through Ludwig v. John-
son 	Controls, 	Inc., 	36 	F.3d 	1396, 	1407 	(8th 	Cir.1994)). 	As 	Dr.
Bergeron 	explained 	the 	basis 	for 	his 	testimony 	and 	Alcor 	had 	a
fair 	opportunity 	for 	cross-examination, 	the 	Court 	does 	not 	find
that 	this 	testimony 	“serious[ly] 	affected 	the 	fairness 	. 	. 	. 	of
the judicial proceedings.” 	Fed. R. Evid. 103(d); United States v.
Gandia-Maysonet, 227 F.3d 1, 5 (1st Cir. 2000).
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its fourth-degree polynomial equation - roughly five months – cor-
roborates this conclusion. 	See § III.B.2, supra.
Extrapolating 	from 	these 	facts, 	Alifax 	argued 	that, 	but 	for
Alcor’s misappropriation, it would have taken several more months
to develop a functional iSED prototype. 	Trial Tr. vol. 12, 55:14-
22. 	Months 	of 	delay 	would 	have 	meant 	missing 	the 	2012 	AACC 	trade
show; 	missing 	the 	trade 	should 	would 	have 	delayed 	the 	debut 	of 	a
new 	instrument 	until 	2013. 	Id. 	46:18-47:5. 	Simply 	put, 	Alifax
argues 	that 	a 	modest 	delay 	would 	have 	sparked 	a 	chain 	reaction.
Thus, 	one 	year 	of 	profits 	attributable 	to 	its 	unfair 	head 	start
was a rational measure of damages. 	See id. 	49:18-21; 54:14-55:9.
An 	estimated 	$6.5 	million 	in 	net 	profits 	from 	iSED-related 	sales
during 	2018 	(a 	year 	in 	which 	Alcor 	would 	not 	have 	earned 	such
revenues 	absent 	misappropriation) 	can 	be 	derived 	through 	simple
arithmetic using the financial data from a spreadsheet created by
Alcor and introduced through Alifax’s only damages witness, Chris-
topher Bokhart.31 See Trial Ex. 173; Trial Tr. vol. 11, 65:7-66:14;
68:22-70:17, May 1, 2019.
“[C]ausation 	can 	be 	shown 	from 	reasonable 	inferences 	drawn
from circumstantial evidence.” 	Melvin F. Jager, Trade Secret Law
§ 7:29 (2019); see also Cartel Asset Mgt. v. Ocwen Fin. Corp., 249
31 	As 	the 	Court 	explains 	below, 	the 	Court 	should 	have 	more
strictly cabined Bokhart’s testimony, which in part warrants a new
trial. 	More on that to come.
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Fed. Appx. 63, 75 (10th Cir. 2007) (“A conclusion concerning cau-
sation may result from a fact-finder's “reasonable inferences from
the 	circumstantial 	evidence 	presented.”). 	Alifax’s 	argument 	for
head 	start 	damages 	is 	– 	like 	the 	rest 	of 	its 	case 	– 	thoroughly
circumstantial. 	It 	is 	not, 	however, 	wholly 	unreasonable. 	The
statements from Ruggeri and Frappa show an urgent desire to launch
the 	iSED 	at 	the 	2012 	AACC. 	Dr. 	Bergeron’s 	testimony 	and 	Alcor’s
own algorithm development timeline suggest that it would have taken
more time than Alcor had available to create a conversion algorithm
and 	claim 	it 	had 	a 	functioning 	device. 	A 	year-long 	delay 	is 	one
outcome that may be reasonably inferred from the trial evidence.
To sum up, the Court concludes that there was legally suffi-
cient evidence at trial to support the jury’s verdict that Alifax’s
conversion algorithm with its four specific constants comprised a
trade secret that was willfully misappropriated by the Defendants.
The 	jury’s 	award 	of 	$6.5 	million 	was 	a 	rational 	appraisal 	of 	Al-
cor’s 	unjust 	enrichment. 	Accordingly, 	Alcor’s 	Rule 	50(b) 	motion
with respect to liability for misappropriation of this trade secret
must be denied.
4. 	The 	Verdict 	Finding 	Misappropriation 	of 	Alifax’s
Conversion Algorithm Is Against the Clear Weight of
the Evidence, Warranting a New Trial.
A critical assumption underpins the jury’s verdict: Alifax’s
algorithm 	was 	capable 	of 	producing 	highly 	accurate 	results 	in 	a
non-Alifax device. 	The Defendants challenged this premise at every
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turn. 	At trial, they relied on the testimony of embedded systems
expert 	Daniel 	Smith.32 	See 	generally 	Trial 	Tr. 	vol. 	8, 	21:12-17,
53-66. 	Smith’s 	background 	included 	years 	of 	diverse 	experiences
as 	an 	embedded 	systems 	engineer. 	He 	worked 	with 	or 	for 	numerous
technology companies, taught several courses on developing embed-
ded systems (including source code development), and had some ex-
pertise 	in 	designing 	medical 	devices. 	Id. 	at 	14:7-19:12. 	His
employment history included serving as the director of engineering
for Tesla Electronics (where he was responsible for designing its
vehicle’s 	electronics 	and 	firmware) 	and 	as 	a 	lead 	engineer 	for
Motorola. 	Id. at 16:25-18:12, 19:13-20:3. 	In the Court’s opinion,
these 	credentials 	made 	Smith’s 	area 	of 	expertise 	a 	superior 	fit
for this dispute.
Smith opined that Alifax’s conversion algorithm and its four
specific constants were, within a reasonable degree of engineering
certainty, incapable of “produc[ing] accurate, meaningful ESR val-
ues in an iSED device[.]” 	Id. at 66:25. 	He designed a method to
test 	his 	hypothesis. 	The 	June 	2013 	Rhode 	Island 	Hospital 	test
data included the aggregation index (a value based on raw optical
density 	data) 	for 	each 	blood 	sample. 	Id. 	at 	58:1-7;
32 	Smith 	defined 	such 	a 	system 	as 	“an 	electronic 	system 	with
an embedded microprocessor that has a dedicated function.” 	Trial
Tr. vol. 8, 13:19-21. 	ESR analyzers satisfy these criteria. 	Id.
at 14:3-5.
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see 	Trial 	Ex. 	484. 	This 	value 	is 	determined 	through 	the 	well-
known, non-proprietary principles of syllectometry and is the sa-
lient input for an ESR analyzer’s conversion algorithm. 	Trial Tr.
vol. 3, 143:20-144:13. Smith’s analysis compared the outputs gen-
erated by the respective algorithms of Alcor and Alifax when this
aggregation 	data 	was 	used 	as 	a 	common 	input. 	Id. 	at 	54:23-56:5.
Put another way, Smith tested the accuracy of Alifax’s claim that
Alcor 	could 	have 	implanted 	its 	conversion 	algorithm 	into 	Alcor
hardware 	and 	produced 	ESR 	values 	highly 	correlated 	to 	Westergren
results.
Using 	the 	Microsoft 	Excel 	software 	program, 	he 	created 	a
spreadsheet 	with 	formulas. 	See 	Trial 	Tr. 	56:17-57:10, 	61:5-15.
Trial 	Ex. 	505. 	For 	each 	sample, 	the 	entry 	included 	(1) 	the
sample’s 	iSED-generated 	aggregation 	index 	(“Integral 	iSED”); 	(2)
an 	ESR 	value 	calculated 	using 	Alcor’s 	conversion 	algorithm 	as 	of
January 	28, 	2013 	(“iSED 	ESR”); 	(3) 	an 	ESR value 	calculated 	using
Alifax’s 	proprietary 	algorithm 	(“ALIFAX 	ESR”); 	and 	(4) 	the 	sam-
ple’s 	ESR 	value 	obtained 	from 	the 	traditional 	Westergren 	method
(“WG”). 	See Trial Ex. 505; Trial Tr. vol. 8, at 62:25-66:2. 	The
maximum acceptable ESR value produced by the Westergren method is
180 	mm/h. 	Trial 	Tr. 	vol. 	8, 	66:5-8. 	Smith’s 	results 	speak 	for
themselves:
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Trial. Ex. 505. 	These first entries typify Smith’s findings. 	When
aggregation data is measured by an Alcor iSED but converted to an
ESR 	value 	using 	Alifax’s 	algorithm, 	the 	instrument 	yields 	worth-
less 	results. 	Id.; 	see 	also 	Trial 	Tr. 	vol. 	8, 	66:13-18. 	The
instrument-generated 	values 	are 	in 	many 	entries 	an 	order 	of 	mag-
nitude larger than the highest permissible Westergren value. 	See
Trial 	Ex. 	505. 	Smith 	concluded 	from 	this 	analysis 	that 	no 	mean-
ingful results could be obtained if Alcor used Alifax’s algorithm
in an iSED. 	Id. at Trial Tr. vol. 8, 66:19-25. 	Conversion algo-
rithms are “device-specific.” 	Id. at 21:12-17.
Alifax 	failed 	to 	challenge 	this 	opinion 	in 	any 	serious 	way.
Its cross-examination largely concentrated on the timeline of Al-
cor’s code development and relied on files produced outside Alcor’s
version 	control 	repository. 	Both 	Smith 	and 	Dr. 	Bergeron 	agreed
that information contained in such files could not be anchored to
a point in time. 	Trial Tr. vol. 4, 20:21-14; vol. 8, at 92:24-9.
To 	be 	clear: 	the 	Court 	is 	not 	choosing 	to 	credit 	Smith’s 	opinion
over Dr. Bergeron’s. 	Alifax did not ask Dr. Bergeron (who watched
Smith’s testimony) or anyone else to provide a rebuttal opinion or
critique Smith’s methodology. 	In fact, on direct examination Dr.
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Bergeron 	stated 	that 	he 	observed 	that 	Alifax 	did 	not 	employ 	the
same 	constants 	consistently 	in 	different 	models 	of 	its 	instru-
ments. 	Trial 	Tr. 	vol 	3, 	at 	124:2-20. 	He 	declined 	to 	identify
changing hardware as the cause of these variations but acknowledged
that 	“it 	[was] 	an 	assumption 	[he 	was] 	making 	. 	. 	. 	”. 	Id. 	at
124:23. 	Thus, even Dr. Bergeron appears to have assumed based on
his considerable education, experience, and observations that con-
version algorithms have some degree of device specificity.
Neither juries nor courts should casually dismiss potent and
unrefuted scientific proof. 	Roma v. Thames River Specialties Co.,
96 	A. 	169 	(Conn. 	1915) 	(holding 	a 	trial 	judge 	“would 	have 	failed
in his duty” if he had not set aside the verdict when, among other
things, “the laws of mechanics, as testified to and uncontradicted,
tended to prove [the claimant’s] story impossible”). 	Alifax argues
– correctly – that the jury was free to reject Smith’s testimony.
See 	New 	Trial 	Opp’n 	15. 	However, 	its 	apparent 	decision 	to 	do 	so
absent 	any 	reasonable 	challenge 	to 	the 	basis 	for 	his 	opinions 	or
an 	alternative 	explanation 	for 	his 	findings 	raises 	insuperable
doubts 	about 	the 	verdict’s 	soundness. 	See 	Venturelli 	v. 	Cincin-
nati, Inc., 850 F.2d 825, 833 (1st Cir. 1988) (stating a new trial
may 	be 	ordered 	on 	appeal 	where 	verdict 	relies 	on 	evidence 	that
“flies 	in 	the 	teeth 	of 	unimpeachable 	contradicting 	evidence 	and
universal 	experience”); 	Kansas 	City 	Pub. 	Serv. 	Co. 	v. 	Shephard,
184 F.2d 945, 947 (10th Cir. 1950) (“Plaintiff cannot prevail . .
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. if the evidence on which he relies is in irreconcilable conflict
with 	immutable 	laws 	of 	physics 	or 	is 	wholly 	inconsistent 	with
established and uncontroverted physical facts”).
If 	conversion 	algorithms 	are 	device 	specific, 	Alifax’s 	ex-
planation 	of 	Trial 	Exhibit 	92 	breaks 	down. 	The 	record 	contains
further 	corroborating 	evidence 	that 	Alifax’s 	algorithm 	could 	not
have been used to achieve those results. 	Sacchetti testified that
Alcor 	assigned 	every 	iSED 	instrument 	a 	sequential 	serial 	number.
See 	Trial 	Tr. 	vol. 	4., 	37:1-4; 	Trial 	Ex. 	138. 	Serial 	numbers
00001, 	00002, 	and 	00003 	were 	prototypes. 	Trial 	Ex. 	138. 	The
instrument 	printouts 	displaying 	ESR 	values 	attached 	to 	Frappa’s
protocol 	were 	generated 	by 	iSED 	number 	“00027.” 	Trial 	Ex. 	92.
Alcor did not manufacture that instrument until June 2013, around
the 	time 	Rhode 	Island 	Hospital 	was 	conducting 	its 	correlation
tests. 	See Trial Tr. vol. 6, 38:22-25; Trial Ex. 138. 	There was
also 	testimony 	that 	the 	date 	on 	the 	printouts 	reflects 	test 	in-
strument’s internal clock, which may have been incorrectly set by
Frappa 	when 	conducting 	the 	tests. 	See 	Frappa 	Dep. 	at 	57:11-13,
63:25-64:6; 	Trial 	Tr. 	vol. 	5 	at 	67:6-10, 	vol. 	6 	at 	35:19-36:16.
Consequently, 	Frappa’s 	handwritten 	dates 	could 	reflect 	the
printouts’ filenames rather than when he ran the tests.
Like 	toppling 	dominos, 	these 	faltering 	arguments 	exacerbate
other 	weaknesses 	in 	Alifax’s 	proof. 	Alifax’s 	interpretation 	of
the phrase “fully functional prototype” in Ecker’s August 6, 2012
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internal 	email 	ignores 	relevant 	context. 	In 	the 	proceeding 	sen-
tence, 	Ecker 	expressly 	states 	that 	while 	the 	iSED 	is 	“fast 	ap-
proaching final stages,” it is “still in development.” 	Trial Ex.
82. 	Consistent 	with 	Ecker’s 	email, 	Ruggeri 	explained 	that 	Alcor
“didn’t 	wait” 	for 	its 	“final 	product” 	– 	i.e., 	a 	device 	that 	gen-
erated reliable ESR values – before laying the groundwork for the
iSED’s 	potential 	sales. 	Ruggeri 	Dep. 	at 	144:15-20. 	So-called
“premarketing” 	activities 	such 	as 	advertisements 	and 	sales 	calls
began 	immediately 	after 	the 	2012 	AACC 	trade 	show. 	Id. 	144:4-20.
Alcor 	would 	not 	roll 	out 	production 	machines 	for 	at 	least 	six
months. 	Id. at 144:4-7.
The 	statements 	from 	Ecker 	and 	Ruggeri 	are 	consistent 	with
Frappa’s 	trial 	testimony. 	Alcor’s 	goal 	for 	the 	2012 	AACC 	trade
show 	was 	to 	produce 	a 	prototype 	showing 	how 	easy 	the 	iSED 	was 	to
use. 	Trial Tr. vol. 7, 60:21-23, Apr. 25, 2019. 	The prototype’s
software 	was 	designed 	to 	demonstrate 	only 	the 	loading, 	identifi-
cation, 	mixing, 	and 	ejection 	of 	blood 	sample 	tubes. 	Id. 	61:19-
62:2. 	The 	tubes 	were 	empty; 	nothing 	was 	measured 	and 	a 	“dummy”
ESR value was reported. 	Trial Tr. vol. 62:1-8. 	Alcor introduced
a 	video 	of 	Frappa 	testing 	a 	prototype 	device 	one 	day 	before 	the
show. Trial Ex. 73. 	The video corresponds to his description and
shows 	Frappa 	using 	a 	prototype 	instrument 	simulating 	the 	end-
user’s 	experience 	with 	empty 	tubes 	and 	a 	randomly 	generated 	ESR
value. 	See 	id.; 	see 	also 	Trial 	Tr. 	vol. 	7, 	at 	62:13-65:16.
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Frappa’s testimony and the video are consistent with Alcor’s con-
temporaneous advertising copy, which emphasizes the iSED’s “set it
and 	forget 	it” 	features. 	See, 	e.g., 	Trial 	Ex. 	82, 	77, 	79. 	None
of these ads claim that the iSED obtains ESR values in a novel or
noteworthy way.
The record of Alcor’s development of the iSED’s reading cell
further undermines the reasonableness of any inference that Alcor
used 	Alifax’s 	algorithm 	for 	any 	purpose 	in 	or 	around 	June 	2012.
Alcor 	engaged 	with 	a 	Chinese 	injection 	mold 	manufacturer 	for 	six
to 	eight 	months 	to 	perfect 	the 	design 	of 	its 	reading 	cell. 	See
Trial 	Tr. 	vol. 	8, 	10:18-11:7, 	Apr. 	26, 	2019; 	Trial 	Ex. 	96.
Frappa’s correspondence shows that Alcor did not even begin working
with 	the 	manufacturer 	until 	mid-September 	2012. 	Trial 	Ex. 	96 	at
ALCOR-0073477. 	The 	company 	sent 	sample 	reading 	cells 	in 	January
2013. 	Id. 	at 	ALCOR-0073459. 	It 	is 	undisputed 	that 	the 	optical
density measurements necessary to obtain an ESR value are made in
the 	instrument’s 	reading 	cell. 	See, 	e.g., 	Trial 	Tr. 	vol. 	3, 	at
34:2-18. 	If 	Alcor’s 	reading 	cell 	development 	did 	not 	even 	begin
until 	September 	2012, 	it 	is 	unreasonable 	to 	infer 	that 	it 	could
make any use of Alifax’s conversion algorithm three months earlier.
One 	more 	omission 	is 	worth 	noting. 	The 	parties 	repeatedly
clashed over the disclosure of their respective source code files.
Alifax’s expert had access to Alcor’s Bitbucket repository as well
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as additional files. Trial Tr. vol. 4, 17:6-18:8. 	And yet, “Ver-
sion 	1.0” 	of 	Alcor’s 	source 	code 	remains 	a 	mystery. 	This 	is 	the
code referenced in Frappa’s protocol attached to the Disputed Cor-
relation 	Tests. 	See 	Trial 	Ex. 	92. 	None 	of 	the 	evidence 	Alifax
identified as code containing Alifax’s conversion algorithm – Ver-
sion 	1.00A 	from 	November 	6, 	2012 	and 	the 	code 	in 	a 	file 	titled
1.04A – has that designation. 	See Trial Exs. 65, 156.
They jury’s verdict that the Defendants misappropriated Ali-
fax’s algorithm and thereby obtained a one-year head start in the
market 	relies 	on 	extensive, 	inference-driven 	reverse 	engineering
from a wafer thin factual. 	A rational fact finder could reach the
same 	result 	as 	the 	jury. 	Nonetheless, 	achieving 	that 	outcome
requires 	rejecting 	powerful 	expert 	testimony 	and 	a 	motherload 	of
contrary 	evidence. 	These 	exceptional 	circumstances 	persuade 	the
Court to excise its discretion under Rule 59 to order a new trial
concerning 	whether 	the 	Defendants 	willfully 	misappropriated 	Ali-
fax’s proprietary conversion algorithm in violation of RIUTSA.
5. 	A New Trial On Damages Is Necessary To Remedy Unfair
Prejudice.
A 	new 	trial 	would 	be 	required 	on 	damages 	even 	if 	the 	jury’s
verdict on liability for misappropriation of the conversion algo-
rithm survived.
Christopher 	Bokhart 	served 	as 	Alifax’s 	sole 	witness 	during
the 	trial’s 	damages 	phase. 	Alifax 	originally 	identified 	Bokhart
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as an expert who would opine as to damages attributable to each of
its 	legal 	claims. 	In 	a 	series 	of 	rulings, 	however, 	the 	Court
excluded all of Bokhart’s opinions. 	See generally Alifax Holding
SpA v. Alcor Sci. Inc., 2019 WL 1930763, *1 (Apr. 30, 2019); Alifax
Holding 	SPA 	v. 	ALCOR 	Sci. 	Inc., 	2019 	WL 	1579503, 	*1 	(Apr. 	12,
2019). 	The 	Court 	issued 	its 	final 	ruling 	mid-trial. 	The 	Court
nonetheless understood that Bokhart reviewed Alcor’s financial in-
formation in the course of preparing his opinions. 	With the intent
of encouraging both practicality and fairness, the Court permitted
Alifax 	(over 	the 	Defendants’ 	objection) 	to 	call 	Bokhart 	pursuant
to Rule 1006 of the Federal Rules of Civil Procedure to testify as
a summary fact witness concerning Alcor’s iSED-related gross rev-
enues. 	Trial 	Tr. 	vol. 	11, 	at 	20:11-22, 	33:10-25. 	The 	Court’s
ruling 	neither 	allowed 	nor 	intended 	to 	allow 	Bokhart 	to 	provide
the jury with any opinion evidence. 	As set forth above, the jury
returned an award that closely parallel’s Alifax’s theory of head
start damages based on his testimony. 	See § III.B.3, supra.
Under 	Rule 	1006, 	a 	party 	may 	“use 	a 	summary 	. 	. 	. 	to 	prove
the 	content 	of 	voluminous 	writings, 	recordings, 	or 	photographs
that 	cannot 	be 	conveniently 	examined 	in 	court.” 	The 	summary 	may
be comprised of a writing or witness testimony. 	See United States
v. Casas, 356 F.3d 104, 119 (1st Cir. 2004). 	Regardless of whether
such evidence is offered by an expert or a lay witness, Rule 1006
is not a backdoor for admitting otherwise impermissible opinions.
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See 	Fagiola 	v. 	Natl. 	Gypsum 	Co. 	AC 	& 	S., 	906 	F.2d 	53, 	57 	(2d
Cir.1990) 	(“A summary must of course be based on foundation tes-
timony connecting it with the underlying evidence summarized, and
must be based upon and fairly represent competent evidence already
before 	the 	jury…”); 	United 	States 	v. 	Radseck, 	718 	F.2d 	233, 	239
(7th 	Cir.1983) 	(“The 	nature 	of 	a 	summary 	witness’s 	testimony 	re-
quires that he draw conclusions based upon the evidence presented
at trial.”). 	Hence, First Circuit has explained that “the key to
admissibility is that the summary witness’s testimony does no more
than analyze facts already introduced into evidence . . . ”. United
States 	v. 	Stierhoff, 	549 	F.3d 	19, 	28 	(1st 	Cir. 	2008) 	(emphasis
added).
Alcor 	made 	vociferous 	objections 	to 	Bokhart 	testifying 	at
trial. 	See, 	e.g., 	Trial 	Tr. 	vol. 	11, 	20:23-14. 	Alcor 	argued 	at
that time (as it argues now) that Bokhart’s testimony should have
been 	excluded. 	See 	Mot. 	for 	New 	Trial 	38-39, 	43-44. 	Again, 	with
the benefit of hindsight and a close review of testimony, the Court
concludes 	that 	those 	objections 	should 	have 	been 	sustained. 	Bo-
khart’s 	knowledge 	of 	facts 	concerning 	Alcor’s 	revenues 	was 	too
closely 	entwined 	with 	his 	excluded 	expert 	opinion 	to 	be 	cleanly
dissected and presented under Rule 1006.
First, the documents and materials Bokhart purported to sum-
marize 	were 	not 	already 	“competent 	evidence 	already 	before 	the
jury.” 	Radseck, 718 F.2d at 239; see also Stierhoff, 549 F.3d at
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28. 	He testified with candor that his “understanding” of Alcor’s
iSED-related revenues were based on “thousands of documents,” in-
cluding 	Alifax 	and 	Alcor 	business 	records, 	marketing 	materials,
business proposals, and financial statements. 	Trial Tr. vol. 11,
at 	45:17-20. 	He 	read 	“depositions 	of 	various 	employees 	of 	both
companies.” 	Id. 	at 	23-24. 	And 	he 	agreed 	that 	his 	testimony
concerning 	“the 	revenues 	and 	profits” 	Alcor 	obtained 	from 	iSED
analyzers 	was 	based 	on 	his 	review 	of 	all 	of 	these 	materials 	and
“discussions with various persons who are on both sides,” including
Alifax 	CEO 	Paulo 	Galiano. 	Id. 	43:21-44:8. 	Just 	one 	of 	these
primary sources was put before the jury: Trial Exhibit 173, a copy
of 	an 	Alcor 	financial 	statement.33 	See 	Trial 	Ex. 	173; 	Trial 	Tr.
vol. 11, at 63:3-16. 	A basic prerequisite of Rule 1006 was there-
fore unsatisfied.
Second, Bokhart’s testimony necessarily reflected the appli-
cation of his financial and accounting expertise to interpret the
evidence. 	This was impermissible. 	For example, he explained that
Alcor three or four financial statements that “didn’t always agree”
and 	that 	there 	were 	“inconsistencies 	from 	document 	to 	document
. 	. 	. 	”. 	Trial 	Tr. 	vol. 	11, 	at 	44:9-17. 	He 	also 	testified 	that
sales 	numbers 	“only 	give[] 	part 	of 	the 	picture. 	You 	have 	to
33 	Trial 	Exhibit 	198 	was 	also 	introduced 	through 	Bokhart 	but
was 	comprised 	of 	an 	attachment 	to 	Bokhart’s 	expert 	report 	summa-
rizing his findings.
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understand 	what 	that 	item 	is 	. 	. 	. 	that’s 	where 	the 	review 	and
understanding of the underlying business documents come into play
in interpreting financial statements.” 	Id. at 44:18-23. 	He came
to 	his 	“understanding” 	based 	on 	all 	his 	“work 	in 	in 	this 	litiga-
tion,” id. at 50:19. 	That is, through his work as an expert.
Alifax’s 	evidence 	about 	convoyed 	sales 	illustrates 	the
Court’s 	concern. 	Bokhart 	offered 	testimony 	about 	objects 	called
“test cards.” 	He told the jury these were items “used to make the
iSED operational,” thus the revenues they generated should be con-
sidered 	iSED-related. 	See 	id. 	at 	50:9-22, 	64:22-65:1. 	Test-card
related 	revenues 	were 	“close 	to 	four 	million 	[dollars].” 	Id. 	at
67:24-68:4. 	He 	provided 	similar 	evidence 	regarding 	“diagnostic
services.” 	See, 	e.g., 	id. 	at 	50:18-51:5, 	57:4-10, 	64:22-65:1,
68:9-11. 	At 	the 	time 	of 	Bokhart’s 	testimony, 	however, 	there 	was
no 	evidence 	from 	any 	other 	witness 	about 	test 	cards, 	diagnostic
services or any other ancillary products that allegedly generated
iSED-related 	revenues. 	None 	of 	this 	testimony 	was 	permissible
within the strict confines of Rule 1006.34
34 	Although 	Alcor 	argues 	at 	length 	about 	excluding 	Bokhart’s
testimony 	as 	improper 	lay 	opinion, 	Rule 	701 	was 	never 	the 	basis
for 	the 	Court’s 	ruling 	and 	would 	provide 	no 	support 	for 	allowing
this 	evidence. 	See 	A.J. 	Amer 	Agency, 	Inc. 	v. 	Astonish 	Results,
LLC, 	C.A. 	No. 	12–351 	S, 	2014 	WL 	3496964 	at 	*22 	(D.R.I. 	July 	11,
2014) (stating a lay witness may testify under Rule 701 regarding
a 	party’s 	financial 	information “based 	on 	the 	witness’s 	own 	per-
ceptions and knowledge and participation in the day-to-day affairs
of the business.”).
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The Seventh Circuit has recognized that in tax evasion pros-
ecutions “the line between summary testimony and expert testimony
is 	indistinct.” 	United 	States 	v. 	Pree, 	408 	F.3d 	855, 	869 	(7th
Cir. 	2005). 	The 	Court 	has 	found 	no 	binding 	precedent 	suggesting
that such hybrid testimony is permissible in a different context.
It 	will 	not 	expand 	this 	doctrine 	here. 	See 	United 	States 	v.
McElroy, 	587 	F.3d 	73, 	82 	(1st 	Cir. 	2009) 	(urging 	“caution” 	with
summary witness testimony and stating “such witnesses are allowed
only 	in 	limited 	situations”). 	Bokhart’s 	testimony 	exceeded 	the
scope 	permitted 	by 	Rule 	1006, 	unfairly 	prejudicing 	Alcor.35 	Per-
mitting the jury’s damages award to stand would constitute a mis-
carriage of justice. 	Therefore, it must be vacated in favor of a
new trial.
IV. 	Conclusion
For 	the 	foregoing 	reasons, 	Alcor’s 	Renewed 	Motion 	for 	Judg-
ment As A Matter of Law (ECF No. 304) is GRANTED IN PART AND DENIED
IN PART. 	Judgment as a matter of law shall enter for the Defendants
on 	Count 	II 	regarding 	the 	claim 	of 	“[u]sing 	a 	clear, 	plastic 	ca-
pillary photometer sensor (“CPS”) in an automated ESR analyzer” in
violation of the Rhode Island Uniform Trade Secrets Act (“RIUTSA”),
35 The Court is neither intending to suggest nor has any reason
to 	believe 	that 	either 	Bokhart 	or 	Alifax’s 	counsel 	intentionally
expanded 	the 	scope 	of 	his 	testimony. 	The 	fog 	surrounding 	this
issue was thick and the boundary was less than obvious.
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R.I. Gen. Laws § 6-41-1 et seq. 	In all other respects, the motion
is DENIED.
Alcor’s 	Motion 	for 	a 	New 	Trial, 	Or 	In 	the 	Alternative, 	For
Remittitur 	(ECF 	No. 	303) 	is 	GRANTED 	IN 	PART 	AND 	DENIED 	IN 	PART.
If judgment is not entered for the Defendants with respect to the
CPS-related trade secret, the Court hereby provisionally orders a
new trial with respect to that allegation. 	The Court furthermore
orders a new trial regarding the Defendants’ liability for alleg-
edly 	misappropriating 	Alifax’s 	proprietary 	conversion 	algorithm
and 	damages 	attributable 	to 	that 	alleged 	harm 	under 	RIUTSA. 	In
all other respects, the motion is DENIED.
In 	as 	much 	as 	a 	new 	trial 	is 	required 	with 	respect 	to 	the
claim of misappropriation of Alifax’s secret conversion algorithm,
the 	case 	will 	be 	returned 	to 	the 	trial 	calendar. 	Final 	judgment
will not enter until all claims are decided.
IT IS SO ORDERED.
William E. Smith
Chief Judge
Date: September 5, 2019
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