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GVP Module I: Pharmacovigilance Systems and their Quality Systems


If you’re looking to get to grips with the regulations and guidelines for pharmacovigilance systems and their quality systems, this course will provide you with a good introduction and equip you with the fundamental principles of Pharmacovigilance.

The course is written by pharmacovigilance professionals working in the pharmaceutical industry and has been reviewed by expert peers prior to release. We are pleased to be able to offer you training that you can complete when and where is most convenient for you.

This course provides a comprehensive overview of Module I (Pharmacovigilance Systems and their Quality Systems) of the Guideline on Good Pharmacovigilance Practices released by the European Medicines Agency in June 2012.

This course is primarily aimed at individuals who are either new to Pharmacovigilance or who work in departments within the pharmaceutical industry that work closely with drug safety e.g. all Medical Information professionals. It is also an ideal course for those providing medical review and for PV professionals with a number of years of experience, but who would like a refresher and/or require evidence of their training on, and understanding of, the GVP Modules.

The course includes a test of understanding to obtain a formal certificate as evidence of training.

Target audience: New PV professionals. Individuals in departments that work closely with PV. Those providing medical review
PV professionals with a number of years of experience, but who require refresher and/or evidence of training on GVP Module VI

Level of difficulty: Introductory / intermediate

Time: 1 -2 hours