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Essentials of European Pharmaceutical Regulatory Affairs




At Your Desk


06 Aug 2020

Reference No: T2006408-TOP

Apply for this event

Key points about this Training Event

  • Get a complete grounding in regulatory affairs in just one day
  • Understand the regulatory affairs sector and find out for yourself how you can maximise your performance, either as a regulatory professional or working alongside regulatory colleagues
Event Description

Course Outline:

This popular course provides an opportunity that on-the-job learning doesn't: network and learn from a variety of experts, including your fellow delegates. By attending this course, you will:

  • Get a clear understanding of the roles played by regulatory affairs professionals obtaining and maintaining marketing authorisation for medicines
  • Learn the key steps involved in developing new pharmaceuticals
  • Gain an overview of EU legislative framework and regulatory procedures
  • Get insights about the strategies needed to be applied by regulatory affairs professionals to obtain best results for their organisations and stakeholders
  • Understand life-cycle management procedures including variations, the essentials of clinical trials and importance of labeling

When & Where?

6 August 2020
09:30 - 16:00

At Your Desk


£580.00 plus 20% VAT


Applicant Requirements
  • Those who are new to regulatory affairs and who wish to move into the profession
  • Those who work in regulatory authorities and those in the regulatory sector
Reference No: T2006408-TOP
TOPRA is the professional membership organisation for individuals working in healthcare regulatory affairs.
We work with our members internationally to enable and promote excellence across the healthcare regulatory profession.


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