European Medicines Agency veterinary medicines info day

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TitleEuropean Medicines Agency veterinary medicines info day
Date16/03/2017 - 17/03/2017
LocationEuropean Medicines Agency, London, UK
SummaryThe European Medicines Agency veterinary medicines info day, organised in collaboration with International Federation for Animal Health Europe (IFAH-Europe), provides first-hand information on the latest developments in the scientific review, regulation and marketing authorisation procedure in the field of veterinary medicine regulation. For the first time, this year, European Medicines Agency (EMA) will have dedicated information points on esubmissions, veterinary application submissions and veterinary medicines innovation.

All documents

Name Language First published Last updated
Agenda - European Medicines Agency veterinary medicines info day (English only) 2016-12-20 2017-03-27
Registration form - European Medicines Agency veterinary medicines info day (English only) 2016-12-20  
Presentation - CVMP achievements 2016 (David Murphy) (English only) 2017-03-27  
Presentation - Anthelmintic resistance (Gesine Hahn) (English only) 2017-03-27  
Presentation - Antimicrobial resistance (AMR): Joint EMA/EFSA RONAFA opinion and harmonisation of SPCs of antimicrobial veterinary medicines (Helen Jukes) (English only) 2017-03-27  
Presentation - Environmental Risk Assessment Recent developments (Chris Van den Eede) (English only) 2017-03-27  
Presentation - EMA/HMA action plan on availability for veterinary vaccines (Faye Ioannou) (English only) 2017-03-27  
Presentation - Availability of veterinary vaccines: Industry perspectives (Frédéric Descamps) (English only) 2017-03-27  
Presentation - Impact of future legislation on availability (Pablo Hervás Calle) (English only) 2017-03-27  
Presentation - EMA Veterinary Portfolio Reviews “Horizon scanning” (Fia Westerholm) (English only) 2017-03-27  
Presentation - How to make legislation more supportive for innovation (Peter Oostenbach) (English only) 2017-03-27  
Presentation - Update on ADVENT and progress on Q&A documents: experience with pre-drafting consultations (Minna Leppänen) (English only) 2017-03-27  
Presentation - Recent experiences with the centralised procedure (Teresa Potter) (English only) 2017-03-27  
Presentation - Best practice guide on adherence to timetables (Piotr Kozarewicz) (English only) 2017-03-27  
Presentation - EMA procedural updates (Emily Drury) (English only) 2017-03-27  
Presentation - How to find the path to SmPC harmonisation? (Caroline Toulemonde, Emmanuelle Royer) (English only) 2017-03-27  
Presentation - Pharmacovigilance and product data (Jos Olaerts) (English only) 2017-03-27  
Presentation - Future Legislation: Pharmacovigilance – Industry vision (Tony Simon) (English only) 2017-03-27  

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Contact point:

IFAH-Europe contacts
Catherine De Norre
IFAH-Europe