813.12OBPFederal Council OrdinanceAug 1, 2005Original source
An application for authorisation of a biocidal product must be submitted to the Notification Authority.
The content of the application shall be in accordance with the following Annexes:
for applications for authorisation ALor AnL: Annex 5;
for applications for simplified authorisation: Annex 6;
for applications for recognition: Annex 7;
for applications for authorisation AN: Annex 8;
for applications for authorisation for parallel trade: Annex 8a .
An application for authorisation of a biocidal product consisting of or containing genetically modified microorganisms must additionally comply with the requirements of the RO1.
The application and documents must be submitted:
in the electronic format specified by the Notification Authority;
in an official language or in English; if the application concerns a biocidal product consisting of or containing genetically modified or pathogenic microorganisms, at least the summary of the application must be written in an official language.
The Notification Authority may, at the request of an assessment authority, require the provision of models or drafts of the packaging, labelling or leaflets.