PHARMACOVIGILANCE
INSPECTIONS FOR THE
VETERINARY INDUSTRY

Conference Date: 11 Feb 2010
Conference Ref: V2-8210
Fee: £550 + VAT
Venue: The Rembrandt Hotel, London

Introduction

European legislative requirements relating to veterinary pharmacovigilance have changed and Competent Authorities have begun carrying out pharmacovigilance inspections. The CVMP began inspections in 2009.

This seminar will address key issues covering: Impact of changing EU legislation, the role of the Qualified Person (QP), preparing for pharmacovigilance audits and inspections, inspection expectations in key areas and interactions with Competent Authorities. This is an excellent opportunity to become fully prepared to handle the changes this legislation has brought to the veterinary industry.

Who Should Attend

Personnel in the veterinary industry from the following departments:

Research and Development, Veterinary Services, Adverse Reaction Monitoring, Regulatory Affairs and Registration. Qualified Persons, Drug Safety Officers and all those involved in the daily practice of pharmacovigilance within the EU will find this seminar beneficial.

Benefits of Attending:

• Understand the European Legislative Requirements for Pharmacovigilance Inspections/Auditing
• Clarify the Role of the Qualified Person (QP)
• Gain Knowledge on Pharmacovigilance Inspections and Competent Authorities Expectations
• Know How to Prepare for Pharmacovigilance Audits

With:

Declan O’Rourke - Ortec Consultancy (formerly Director VMRD, Pfizer Animal Health)
Caroline Evans - Pharmacovigilance Assessor, Veterinary Medicines Directorate (VMD)

Click here to book your place