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Essentials of European Pharmaceutical Regulatory Affairs




London, United Kingdom


05 Aug 2019

Reference No: T1907360 - 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

This course will cover

A clear understanding of the roles played by regulatory affairs professionals obtaining and maintaining marketing authorisation for medicines
Learning the key steps involved in developing new pharmaceuticals
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?

05 August 2019 09:30 - 16:30

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


Course fee for delegates £580.00 plus 20% VAT



Applicant Requirements
  • Those who work in regulatory authorities and those in the regulatory sector
Reference No: T1907360 - 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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