The European Medicines Agency Info Day will take place at the London headquarters from 16-17 March 2017.
The EMA Info Day will focus 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
Antimicrobial resistance (AMR)
Recent developments in environmental assessment
Session II: Availability of veterinary medicines
Industry perspective on action plan
Impact of future legislation on availability
Session III: Innovation
Horizon scanning: General outcome from meetings with industry; Early support for novel types of products (15’)
Innovation: How to make legislation more supportive for innovation (15’)
Update on ADVENT and progress on Q&A documents
Session IV: EU Procedural updates
Recent experiences with centralised procedure: opportunities for development
EMA procedural updates
Session V: Regulatory policy
Future Legislation: harmonisation of SPCs
Future Legislation: pharmacovigilance:
Registration is now closed.