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PMS and Periodic Safety Reports for MedTech & IVD Manufacturers

Thursday 17th November 2016 @ 8:00 am - 5:00 pm

 

Manufacturers of both Medical Devices and In Vitro Diagnostic products will be experiencing significant increases in expectations regarding clinical evidence and PMS. It is imperative that organisations plan now to ensure data is continually gathered, analysed and reported to comply with these new regulations.

Medilink WM, in conjunction with Acclaim Biomedical Consulting, is offering a one day workshop exploring the new requirements for increased PMS. With over 20 years experience in Medical Devices and IVDs, Acclaim Biomedical Consulting are best placed to support and advise on the increased regulatory requirements and the impact these will have on existing practice.

The MPD Training course is designed to review critical elements of the new regulations and will be run as an interactive 1 day course designed for those with a good working knowledge of current requirements.

Who should Attend

 

  • Medical Device Manufacturers
  • IVD Manufacturers
  • Clinical Leaders
  • Regulatory Affairs Officers and Managers
  • Quality Control Officers and Managers

Delegate Fees

Member: £140 + VAT
Non-Member: £190 + VAT

To find out more information or register your place, please click here.

Details

Date:
Thursday 17th November 2016
Time:
8:00 am - 5:00 pm
Event Category:

Organiser

Sarah Wootton
Phone:
0121 452 5630
Email:
sarahw@medilinkwm.co.uk

Venue

MTIC
4 Greenfield Crescent
Birmingham, B15 3BE
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