September 9 - 10, 2014    巴塞罗那 , 西班牙
Speed up your product approval with feedback from 9 national regulators plus critical feedback from the EU Commission

Snap Shot of Topics to be Covered

Revision to the Veterinary Medicines Directive (if published before September)
Marketing Authorisations and Harmonisation across Member States
Filing Variations and Work Sharing
E-Submissions and Dossier Development
Feedback from the EU Commission: Medicated Feed Legislation
Antimicrobial Resistance
Pharmacovigilance
Successfully Registering Generic Veterinary Medicines
Environmental Risk Assessment and Testing Procedures

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