Our extensive team is drawn from consultancy, CROs, industry and government. We have scientific expertise and real practical knowledge relating to Regulation (EU) No. 528/2012 and national requirements relating to biocidal products.
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Biocides
We can assist with
- Strategic advice, including data gap analysis and preliminary risk assessments
- Study placement, generation and monitoring (GLP)
- New active substance authorisations
- Active substance renewals
- Product registrations and renewals, including national or Union authorisation, simplified procedure, mutual recognition, same product procedure
- Transitional registration in all European countries
Our achievements
We have produced and submitted many dossiers for our clients, resulting in positive outcomes for the following areas:
- New active substances
- Renewal of existing active substances
- Approval (and renewal of approval) for multiple formulated products
- Technical equivalence applications
- Risk Assessment refinement
- Proposals for harmonised Classification & Labelling
- Poison Centre Notifications (Art. 45 CLP)
We have also supported clients in:
- Advising on the optimum strategy (costs and lead times) for products
- Pre-submission meetings
- Liaising with authorities
- Post submission stages, including commenting and lobbying
- Advising on data protection issues
Our team can assist you with any regulatory issue. Please do contact us if you need our support or if you would like to find out more.
Our services
Your contacts
Aurély Béghin
Regulatory Affairs Deputy Director
+33 (0)6 26 14 64 99
Sophie Aviron-Violet
Biocides Team Leader
+33 (0)6 84 85 21 42
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