R&D and Tests |
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Written by DPR Biocides - Anses |
Notification of an experiment (see Article 56 point 2 of the BPR) likely to result in the release into the environment of a non-authorised biocidal product or (new) non-approved active substance is sent to ANSES, which maintains a register of these experiments. In the event that the conditions of the experiment would have a negative impact (adverse effects) on humans, animals or the environment, ANSES sends substantiated findings calling for the experiment to be prohibited to the Ministry of the Environment within 45 days of the date of notification. Such an experiment is then subject to a prior "R&D MA" that determines its implementation conditions, after consultation with ANSES (see Article 56 point 3 of the BPR). It is possible to apply directly for an MA without the need for notification.
Comments Notifications for R&D relate solely to products that contain:
R&D notifications do not need to be made for products subject to the provisions of the transitional period (i.e. whose active substances are in the review programme) because these products can be placed on the market according to the national provisions. Regulations: Article 56 of Regulation ( EU) No 528/2012 Timeframe
Validity of the MA: 2 years maximum Fees payable to ANSES
Composition of the dossier It is important to provide a review of the available data. The dossier can therefore be supplemented with any other information deemed useful. |
Last Updated on Thursday, 07 July 2016 15:48 |