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Basics of Pharmacovigilance in Clinical Trials

Overview of PV in Clinical Trials

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Who should attend?

Anyone who wishes to get an overview of basic pharmacovigilance in clinical trials. Especially newcomers in clinical trial pharmacovigilance and/or those working in the pharmaceutical or CRO industry in clinical research.

Details

This workshop is designed to provide a solid foundation of Pharmacovigilance (PV) in Clinical Trials. It will introduce the most important terms and definitions, MedDRA (Medical Dictionary for Regulatory Activities) coding, SAE (Serious Adverse Event) management, unblinding processes, SUSAR (Suspected Unexpected Serious Adverse Reaction) submission, and a first glance at a PV database.

Prices

Early Bird Fee: CHF 990.00 + 7.7% VAT (valid until: 26.02.2019) Regular Fee: CHF 1'100.00 + 7.7% VAT (valid after: 26.02.2019) 10 % reduction for CTC employees, SwAPP and SBA members. The fee includes course documentation, refreshments, lunch and a course participation certificate. For special fees and group discounts please contact training@ctcresourcing.com

Contact

Tamara Kohler
tamara.kohler@ctcresourcing.com

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