Pharmacovigilance
Systems for Drug Development & Post-Marketing SurveillanceMar 15,2010 - Mar 16,2010
Crowne Plaza Hotel, London, England
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Highlights
The importance of developing effective pharmacovigilance systems has been fuelled by an increased focus on drug safety and the ever-changing regulatory environment. This conference will tackle inspections, risk management, the use of Independent Data Monitoring Committees and establishing relationships with regulatory bodies along with a host of other key topics.
Reasons to Attend
• Hear the latest updates on various pharmacovigilance systems in the industry
• Explore ways in which you can optimise your own pharmacovigilance activities
• Discuss the potential impact of impending regulatory changes
• Network with industry associates and discuss experiences
Presentations Include:
• THE FUTURE OF PHARMACOVIGILANCE IN THE EU
Elmar Kroth, Head of Pharmacovigilance, German Medicines Manufacturers' Association
• INTERNAL AUDIT STRATEGY FOR PHARMACOVIGILANCE
Benoit Nauge, Senior Manager, Global Compliance Auditing, Amgen
• PHARMACOVIGILANCE INSPECTIONS BY NATIONAL HEALTH AUTHORITIES
Dominique Brunier, Head of Pharmacovigilance and Quality, Europe, Novartis

Event Reminder
- Registration Open
- Call for Papers
- Call for Speakers
- Receive GTM eblast updates
- Security Code:
Event Profile
- Theme: Systems for Drug Development & Post-Marketing Surveillance
Contact Details
- Contact person: James Brady
- Event website: http://www.smi-online.co.uk/pharmacovigilance9.asp
- Phone: +44 (0) 20 7827 6104
- Fax:
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