Medical Affairs

This practical 2-day introductory-level training course will examine the complex processes involved in meeting the EU regulatory requirements.

Medical & Health Care

Submit new post
Thank you for posting.
Share it:

The European Commission are currently undertaking a further complete Revision (Recast) of the regulatory requirements. Learn about these proposals and the latest developments and how these will affect you in the future

From early decisions regarding the most appropriate conformance route of a product, through to post marketing adverse event reporting, delegates will learn which regulations directly apply to their product and what steps need to be taken to achieve full compliance and ensure patient safety.

Who Should Attend?

-Regulatory Affairs professionals seeking to improve their skills in the regulatory environment
-Those moving into Regulatory Affairs from other areas within a medical device company (Clinical Trials, Marketing and others
- Anyone wishing to update their knowledge on EU regulatory affairs

Book before the 20th August: £1395 + 20% VAT = £1674
Book before the 20th August: £1495 + 20% VAT = £1794

From: September 17, 2014 09:00
To: September 18, 2014 17:00

Radisson Blu Edwardian Grafton Hotel, 130 Tottenham Court Rd, W1T 5AY, United Kingdom


Medical & Health Care


clinical trials, mdd regulations, medical devices, regulatory affairs



Contact email

Contact phone
+44 020 75575784


Submitted by:

evvnt Platform

Are you the organizer?

Get in touch