Harnessing the power of microbial genomics for market authorisation of bioinputs.
Bioinputs are composed of either microorganisms as active substance, or theirby-products. In France, all microorganisms must undergo a rigorous safety evaluation process conducted by the Agence Nationale de Sécurité Sanitaire de l’Alimentation, de l’Environnement et du Travail (ANSES). Applicants are required to compile a dossier substantiating the safety of their product and submit it to ANSES for approval.
Challenges of ANSES Market Authorisation
Navigating the ANSES safety evaluation process presents significant challenges. The procedure is extensive and complex due to the volume of analyses required and the rigorous expectations. Applicants must meticulously compile and present comprehensive data on the safety of the microorganisms used.
This includes detailed scientific evidence, risk assessments, and adherence to strict regulatory standards. The substantial documentation and rigorous scrutiny can be daunting, demanding time, expertise, and resources. Successfully navigating this process is crucial for market approval and ensuring the safety of biofertiliser and biocontrol products.
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