|Written by DPR Biocides - Anses|
|Thursday, 08 April 2010 14:43|
Applications for authorisation (or registration for low-risk products) can be made by an individual or legal entity responsible for the placing on the market of the biocidal product. The applicant must have a permanent office in the European Union, and may be the future holder of the authorisation, or an individual / entity representing the applicant (third-party applicant).
|Last Updated on Friday, 25 March 2011 16:00|