Filing of marketing authorization for a biocidal product

The filing of a marketing authorization for a biocidal product is a regulatory service that accompanies the submission of an MA dossier for a biocide (type TP1 to TP22) according to Regulation (EU) No. 528/2012. It includes analysis of the composition, toxicology, efficacy, labeling, CLP compliance, and regulatory follow-up with the authorities. It is essential for the marketing of biocidal products in Europe.

At YesWeLab , we collaborate with a rigorously selected network of laboratories, most of which are certified and/or accredited (ISO 17025, COFRAC, etc.). These laboratories are chosen based on your specific needs, the matrices to be analyzed, and the analytical techniques or methods required.
If you have any specific requirements, please do not hesitate to specify them when submitting your request: our scientific team makes every effort to respond accurately and responsively.
Since 2020, many manufacturers, distributors, and design offices have trusted us to manage their analyses, entrusting us with their samples via our digital platform.
To find out more or submit a specific need, contact our team now.