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