Pharmacovigilance Working Party
VeterinaryPharmacovigilance
The Pharmacovigilance Working Party (PhVWP-V) provides advice to the Committee for Veterinary Medicinal Products (CVMP) on the co-ordination and supervision of the pharmacovigilance of centrally authorised veterinary medicinal products, as well as of nationally authorised products or products authorised through the mutual recognition procedure.
Responsibilities and composition
The PhVWP-V prepares and updates pharmacovigilance guidelines and provides recommendations on international agreements in the field of pharmacovigilance, particularly through the International Cooperation on Harmonisation of Technical Requirements for Registration of Veterinary Medicinal Products (VICH).
The PhVWP-V is composed of European experts selected according to their specific expertise. It includes one member nominated by each European Union Member State, plus three observers, one nominated each for Iceland, Liechtenstein and Norway.
More information on the PhVWP-V's responsibilities, composition, procedures and activities is available in the following documents:
Members
Below (in alphabetical order of surname) are the current members of the PhVWP-V. The members' declarations of interests are available in the European expert list.