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Essentials of European Pharmaceutical Regulatory Affairs

Price

£580

Location

At Your Desk

Date

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?

When:
6 August 2020
09:30 - 16:00

Where:
At Your Desk

Cost?

£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.

Email info@topra.org

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