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2017 EMA Info Day

London, 16 March 2017
 

The European Medicines Agency Info Day took place at the London headquarters from 16-17 March 2017.

The EMA Info Day focused on the latest developments in scientific review, regulation and marketing authorisation procedures for veterinary medicinal products.

Schedule: 16 March 2017 13:30 PM to 17 March 2017 13:00 PM. 
Programme: Full programme

Session I: Scientific developments
CVMP achievements 2016 - David Murphy
Anthelmintic resistance - Gesine Hahn
Antimicrobial resistance (AMR) - Helen Jukes
Recent developments in environmental assessment - Chris van den Eede

Session II: Availability of veterinary medicines
Vaccine availability - Faye Ioannou
Industry perspective on action plan Frederic Descamps
Impact of future legislation on availability - Pablo Hervas

Session III: Innovation
Horizon scanning: General outcome from meetings with industry; Early support for novel types of products - Fia Westerholm
Innovation: How to make legislation more supportive for innovation - Peter Oostenbach
Update on ADVENT and progress on Q&A documents - Minna Leppanen

Session IV: EU Procedural updates
Recent experiences with centralised procedure: opportunities for development - Teresa Potter
Transparency/communication - 
EMA procedural updates - Emily Drury

Session V: Regulatory policy
Future Legislation: harmonisation of SPCs - Caroline Toulemonde
Future Legislation: pharmacovigilance - Jos Olaerts & Tony Simon

 

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