Download this page in PDF formatBetter regulation for veterinary medicines: Road to a European marketing authorisation
The conference will provide an opportunity for key European decision-makers, regulators, opinion leaders, animal health professionals and other interested parties to discuss opportunities and challenges to improve legislation, decrease the administrative burden of the EU regulatory system and increase the availability of veterinary medicines in the EU.
Provisional topics
- Key findings from the impact assessment
- How do we achieve a European marketing authorisation: CP versus MRP/DCP, harmonisation of existing SPCs and impact on administrative burden
- How to reinforce innovation: new technologies and data protection
- Other opportunities for reducing administrative burden: pharmacovigilance, packaging and labelling
- Reforms needed for medicated feed