General support for registration of biocidal products and active substances

Our experts are involved in the registration of biocidal products since the implementation of Directive 98/8/EC (BDP) and Regulation (EU) no 528/2012 (BPR).

Our experience gives us a strategic overview of the registration of a product range. We can use our scientific expertise to advise you such complex domains as analytical chemistry, effectiveness, toxicology and ecotoxicology.

Redebel Regulatory Affairs (RRA) provides you with effective, efficient support throughout the registration process for your products and substances.

Our main goal is to sustain your product portfolio and market your products within Europe.

Dossier submission: steps

1. Define the project

2. Data Gap Analysis (DGA)

3. Study Monitoring

4. Dossier writing

5. Submissions to relevant authorities

RRA can support you throughout this complex process or simply for one clearly-stated stage.

 Why choose us ?


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