Application for marketing authorization of a biocidal product

The application for marketing authorization of a biocidal product is a regulatory service that accompanies the submission of a marketing authorization dossier for a biocide (type TP1 to TP22) according to Regulation (EU) No 528/2012. It includes analysis of 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 carefully 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 required analytical techniques or methods.
If you have any particular requirements, please do not hesitate to specify them in your request: our scientific team will do everything possible to respond accurately and promptly.
Since 2020, numerous manufacturers, distributors, and engineering firms have entrusted us with the management of their analyses, sending us their samples through our digital platform.
To learn more or submit a specific request, contact our team today.