Commentaries: Art. 13e

Anyone who, for purposes of research and development, handles unauthorised biocidal products or non-approved active substances for use in biocidal products must keep records detailing the following:
1. identity of the biocidal products or active substances;
2. labelling data;
3. quantities supplied;
4. name and address of the person receiving the biocidal products or active substances;
5. all available data concerning possible effects on humans, animals or the environment.
The records shall be made available to the Notification Authority on request.
The Notification Authority may, if necessary, request further information.