Regulatory AffairsBiocidal Products
On 22 May 2012, The EU issued the Biocidal Products Regulation 528/2012 laying down the obligations on Biocidal products licensing procedures. All Biocidal products need to be licensed prior to their placement on the market, following approval of their active ingredient/s.
The demand of biocidal products has grown exponentially due to COVID-19, especially that of disinfectant products and through our experienced network of partners we can offer complete solutions in:
- File preparation for Biocidal Products
- Registration of Biocidal Product files through various Licensing Procedures (Union, National, Mutual and Simplified)
- Biocidal product dossier preparation for:
- Product Types (PT) 1, 2, 3, 4, 5, 6, 7, 11, 20 and 22 approved by the National Competent Health Authorities.
- Product Types (PT) 8, 9, 10, 12, 13, 15, 16, 17, 19, 21 and 23 approved by the Ministry of Rural Development and Food
- Generation of Efficacy tests through collaboration with accredited laboratories
- Generation of physicochemical, toxicological and ecotoxicological data through collaboration with accredited laboratories
- Direct communication and problem solving with the Local Competent Health Authorities for your on-going BP registration.