PHARMACOVIGILANCE
Conference Date: 14 Dec 2009-28 Jan 2010
Conference Ref: A12-1009
Fee: £1595 + VAT
Venue: The Rembrandt Hotel, London
Key topics to be addressed at this conference:
- Principles of Pharmacovigilance and Data Resources
- Risk Management
- Causality Assessment: Clinical Diagnosis of Adverse Events
- Pharmacoepidemiological Studies
- Practical Aspects of compiling PSURs
- Pro-active Pharmacovigilance Pre- and Post Marketing
- Monitoring and Reporting Adverse Reactions in Europe: Regulatory Framework, Clinical Trials, Post-Marketing
- Risk/Benefit Analysis
- Drug Surveillance in the USA & Japan
- Prescription Event Monitoring and its Practical Use in England
- Practical Pharmacovigilance Workshop
- Approaches to organisation of safety surveillance in major pharmaceutical companies
WHY YOU SHOULD ATTEND
This Management Forum course aims to provide basic training for those concerned with pharmacovigilance. New entrants as well as experienced operators in drug safety monitoring will benefit from the mixture of scientific knowledge and practical guidance. In addition, detailed information will be provided on regulatory developments in pharmacovigilance in Europe, the USA, and Japan.
WHO SHOULD ATTEND
This three-day introductory course is aimed at personnel in research and development departments, adverse reaction monitoring units, regulatory affairs and registration departments; pharmaceutical physicians and drug safety officers. It will also be of direct benefit to all those who are involved and interested in the daily practice of pharmacovigilance.

