Scientific advice
Table of contents
The European Medicines Agency can give scientific advice to companies on the appropriate tests and studies in the development of a veterinary medicine. This is designed to facilitate the development and availability of high-quality, effective and acceptably safe medicines.
For veterinary medicines, scientific advice is given by the ">Committee for Medicinal Products for Veterinary Use (CVMP) on the recommendation of the Scientific Advice Working Party (SAWP).
Information on fees payable for scientific advice can be found under fees.
Medicine developers should use EMA's secure online IRIS platform to request scientific advice from EMA:
The IRIS platform provides a single space for applicants and EMA to submit requests, communicate, share information and deliver documents concerning a scientific advice procedure.
Medicine developers first need to complete the registration steps set out in the
Quick interactive guide to IRIS registration process
before using IRIS to apply for scientific advice.
The IRIS platform homepage also explains how to register and make regulatory submissions using IRIS.
The guidance document and template below provide more information on applying for scientific advice.
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European Medicines Agency guidance for companies requesting scientific advice (veterinary) (PDF/321.66 KB)
First published: 01/03/2007
Last updated: 19/10/2020
EMA/CVMP/11887/2020 -
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Scientific advice request template (DOCX/116.36 KB)
First published: 05/04/2017
Last updated: 19/10/2020
EMA/CVMP/SAWP/11888/2020 -
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Veterinary Scientific Advice procedure - submission deadlines 2023 (PDF/100.99 KB)
First published: 05/11/2021
Last updated: 22/11/2022
EMA/CVMP/SAWP/836463/2022