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Essentials of European Pharmaceutical Regulatory Affairs




London, UK


27 Feb 2020

Reference No: T2002393-TOP

Apply for this event

Key points about this Training Event

  • Get a complete grounding in regulatory affairs in just one day
  • Be taught by regulatory affairs experts with extensive practical examples
  • 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
  • Build a network to support the rest of your career
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?

27 February 2020

TOPRA  6th Floor
3 Harbour Exchange
South Quay
London, E14 9GE


Course Fee for Standard Attendee: £580 plus 20% VAT

Applicant Requirements
  • Those who are new to regulatory affairs
  • Those who wish to move into the profession
  • Designed for those from related professions (law, pharmaceutical manufacturing, marketing and sales, healthcare, administration, project management)
  • Those who work in regulatory authorities and those in the regulatory sector
Reference No: T2002393-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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