- Full Dossier preparation for active substances for Annex I inclusion.
- Full Dossier preparation for placing a Biocidal Product in the market.
- Identification of data gaps.
- Contracting studies, including full budgetary responsibility and quotations.
- Study direction and study monitoring.
- Contact with national and EU authorities.
- Pre and post submission support.
- Mutual recognition procedure.
- Safety Data Sheets (SDS), if required.