Pharmacovigilance

A basic training for those working on Drug Safety monitoring in the EU, USA and JAPAN.

1-3 Dec 2014 at The Rembrandt Hotel, United Kingdom

Medical & Health Care, Pharmaceuticals/Drug Discovery

Pharmacovigilance 1-3 Dec 2014 The Rembrandt Hotel, United Kingdom
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KEY TOPICS TO BE ADDRESSED AT THIS CONFERENCE: -

•Principles of Pharmacovigilance and Data Resources
•Risk Management and Risk Minimisation
•Causality Assessment: Clinical Diagnosis of Adverse Events
•PASS and PAES studies
•Regulatory Framework
•European Post-Marketing Pharmacovigilance Regulations
•Pharmacoepidemiological Studies
•Evolution of PSURs, PBRERs, DSURs
•Pro-active Pharmacovigilance Pre- and Post-Marketing
•Clinical Trial ADR reporting requirements
•Risk/Benefit Analysis
•Drug Surveillance in countries outside Europe
•Post-marketing Surveillance: Observational Cohort Studies
•Introduction to Signal detection
•Introduction to Risk Management plans
•Practical Pharmacovigilance Workshop

Price
Standard: GBP 1750

Speakers: Professor Saad Shakir Drug Safety Research Unit, Shelley Ghandi NDA Regulatory Science Ltd, Dr. John Talbot University of Hertfordshire, Dr. John Parkinson CPRD Consultant Expert, Dr. Glyn BelcherPV Consultancy Ltd

When
From: December 01, 2014 09:00
To: December 03, 2014 17:00
Where

The Rembrandt Hotel, SW7 2RS, United Kingdom

Category

Medical & Health Care, Pharmaceuticals/Drug Discovery

Contact email
sarah@management-forum.co.uk

Contact phone
+44 01483 730071

External link

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