Introduction to Regulatory Affairs for Medical Devices

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

9 Jun 2014 at Radisson Blu Edwardian Grafton Hotel, United Kingdom

Medical & Health Care, Management

Introduction to Regulatory Affairs for Medical Devices 9 Jun 2014 Radisson Blu Edwardian Grafton Hotel, United Kingdom
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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.

Course Highlights
•Gain a complete overview of the latest MDD regulations.
•Determine the most appropriate conformance route for your products.
•Meet the requirements for clinical data evaluation.
•Examine the role of risk management throughout the lifecycle of your medical devices.
•Work effectively with EU Regulators to gain clarification.

Price:
Book before the 12th May 2014: £1,395.00 Plus (VAT @ 20.00%) = £1,674.00
Book after the 12th May 2014: £1,495.00 Plus (VAT @ 20.00%) = £1,794.00

When
From: June 09, 2014 09:00
To: June 09, 2014 17:00
Where

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

Category

Medical & Health Care, Management

Contact email
rachael.ouston@informa.com

Contact phone
020 7551 9919

External link

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