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Biocidal Products Regulation

Simplified authorisation

How can a company request an amendment of Annex I of the BPR?
The European Commission has adopted an Implementing Regulation (Commission Implementing Regulation (EU) No 88/2014) specifying the procedure for amending Annex I of the BPR. It clarifies the procedure to be followed when an application is made to include a substance in Annex I.The regulation confirms that the application follows the procedure of Article 7 of the BPR.
The data requirements for the inclusion of an active substance are given in Annex I to Regulation (EU) No 528/2012.
You can find the Implementing Regulation at:
How much are the fees for the simplified authorisation procedure according to the provisions of the BPR and how can a company apply for it?
A simplified authorisation can be requested as of 1 September 2013 if the conditions in Article 25 are satisfied. The fees applicable for the dossier evaluation depend on the competent authorities selected by the applicant for the evaluation process as described in Article 26(2) of the BPR. 
Note that the Commission Implementing Regulation (EU) No 564/2013 of 18 June 2013 concerns only the fees and charges payable to ECHA pursuant to Regulation (EU) No. 528/2012. 
The format acceptable for the submission of a simplified authorisation is a IUCLID file submitted through R4BP 3. Applicants are requested to use the general template for product authorisation by filling in only the relevant parts described under Article 20(1)(b).

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