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
+44 020 75575784