Biocidal product approval requires scientifically justified testing strategies, robust efficacy data, and well-structured regulatory documentation. Authorities expect compliance with EN 14885, OECD guidance, and ECHA requirements for claim substantiation. Our strategic consulting services support testing pathway definition, study design, expert judgement preparation, and technical oversight.
We help manufacturers optimise testing programs, reduce project risk, and strengthen regulatory acceptance of efficacy and safety claims.
Definition of optimised testing strategies aligned with intended claims, Product Types, and regulatory expectations.
Preparation of structured efficacy summaries and technical justifications supporting product authorisation and marketing claims.
Technical oversight of study execution, resultsand deliverable consistency according to regulatory requirements
Preparation of Expert Judgement documents to support regulatory arguments and strengthen dossier completeness.