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Joint MHRA/DIA Excellence in Pharmacovigilance 2017

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

If you would like to register for this conference, or obtain further information or a letter of invitation to this conference, please follow the View Conference Website link above.

Join TheConferenceWebsite here for more Conferences in your Medical Specialty
Join TheConferenceWebsite here for more Conferences in your Medical Specialty