LRQA is pleased to be taking part in The New Medical Device Regulation & IVD Regulation seminar which is taking place from 9-10 October 2014
With all of the uncertainty and change in the regulation of medical device products and in-vitro diagnostics in Europe and beyond, this seminar will bring you the very latest information on what changes have occurred and will look forward to the proposed revision to the medical device legislation, what to expect and how it will affect you. You will hear leading experts discuss the changes and clarify the implications for your company and working practices.
If you are a Manager or Head of Department within a Medical Device company or involved in Regulatory Affairs, Quality Assurance, Clinical Research, Product Design & Development, Vigilance, Safety or PMS, then this event is for you.
Delegates who attend the event will be able to discuss and share information with key industry leaders which will be invaluable in preparation for the forthcoming legislative changes.
Industry expert Theresa Jeary, LRQA's Technical Manager for MDD, will be presenting on the following topics at the event:
- 9 October 2014 from 12.00 to 12.45 - Notified Bodies (NB) - Implications for their Supervision and their Operation
- 9 October 2014 from 14.00 to 14.45 - Unannounced Audits - Notified Body Perspective and Implications for Device Manufacturers
This is a great opportunity for you to expand your knowledge and to learn how LRQA can help you meet your regulatory requirements.
To find out more about the event or to register to attend, please visit Management Forum