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Overview

*Short Courses require an additional registration fee. You do not need to be registered for the forum to attend*


This Short Course will be offered virtually – Join from anywhere!

This course is an introduction to Good Pharmacovigilance Practice (GVP) operations development, from clinical trials to the post-marketing environment. We will examine the laws within the US, EU, and other regions and discuss how to take those requirements and operationalize them into practice at a company. The audience will learn from a real-world example guiding them through the process of starting a safety unit at a small biotech, from staffing and vendor selection, to process implementation and preparing for the post-market experience.


Registered attendees for this virtual Short Course will receive access to the course recording for 2 full months post-course! This allows you to remain flexible with your schedule and not worry if you need to step out momentarily. Have a conflict with the dates of the course, but are interested in the content? Register anyway and you will receive access to the recording!

Receive $150 off your Global Pharmacovigilance and Risk Management Conference registration by registering for at least two short courses and the main conference. Purchases must be made at the same time to receive the discount. Discount will be reflected on the last page of the cart.

Learning objectives

Upon completing this course, attendees will be able to:
  • Discuss the role of the safety department in product development
  • Apply the regulations surrounding companies’ obligations to product safety and surveillance
  • Analyze a real-world scenario to understand the process of implementing a GVP department