Regulation (EC) 726/2004 of the European Parliament and of the Council lays down Community procedures for the authorisation and supervision of medicinal products for human and veterinary use and the establishment of a European Medicines Agency. In February 2007, Volume 6B was published on the presentation and content of the dossier for veterinary medicinal products.
SCC can assist you either with full support of an authorisation process, or take care of certain parts of the process. Over the last 20 years, SCC has had considerable experience in the generation of environmental risk assessments in the area of agrochemicals. For more information on this subject, please use this LINK.
