Joint MHRA/DIA Excellence in Pharmacovigilance 2017
February 27 - March 3, 2017
london , United Kingdom
This course is designed to provide a firm grounding in key aspects of European Clinical Pre- and Post-Marketing Safety regulatory requirements. This five-day training course also includes highlights and updates on the pharmacovigilance legislation and the latest news on the international harmonisation and standardisation activities in pharmacovigilance. What you will learn - Definitions and Methods in Pharmacovigilance - Regulatory Aspects in Pharmacovigilance and Practial Examples - Diagnosis of Adverse Drug Reactions - Signal Detection and Signal Management - Modern Technologies and Social Media - Risk Management
Organizer
DIA Europe
+41 61 225 51 51
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Joint MHRA/DIA Excellence in Pharmacovigilance February 27 - March 3, 2017