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IIR PTI
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| Adverse Event Reporting and Pharmacovigilance |
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Mon 12 Apr 2010
- Tue 13 Apr 2010
Venue to be confirmed, London, England
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COMPLETELY UPDATED FOR 2009!
Recent times have proved to be the most turbulent in pharmacovigilance for many years. With million dollar fines, tougher guidelines and the introduction of MedDRA, it is crucial that you and your company reduce the risk of incorrect ADR reporting...now. This hands-on course is packed with practical examples and industry case studies to give you the confidence to cope with the daily demands of pharmacovigilance.
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The course is ideal. It has an overview of all the important topics in Pharmacovigilance
Drug Safety Scientist, Acteliion
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Who Will Attend?
Regulatory Affairs - Pharmacovigilance - Drug Safety - Products Safety - Medical Affairs - Clinical Safety - Data Management - Drug Surveillance - Medical Information - Post-Marketing Surveillance
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Course Leader
Carol Markwell, Director, Drug Safety Solutions Ltd
Carol has over 14 years management experience in international Drug Safety and has obtained a Postgraduate Diploma in Pharmacovigilance. She has extensive knowledge of drug safety requirements, regulations and practices and has developed and implemented local and international SOPs.
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