We are only a few days away from the #Veterinary #Pharmaceutical Submissions in the EU taking place in #London from 26-27 November! Register now with Medicaleventsguide
This course will take participants through all of the constituent parts of the application for marketing authorization for a veterinary medicinal product in the European Union, including the maximum residue limits dossier.
Presentations will cover the regulatory framework; pharmaceutical, toxicological and pharmacological data; safety risk assessments; pre-clinical and clinical data; detailed and critical summaries; and regulatory submissions. An important part of the program will be devoted to working on case studies in the workshop sessions.
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