The Role of the Qualified Person under the Medical Device Regulations

1-Aug-2013

29 November 2013, Meeting, London, UK

29 November 2013

Meeting

London, UK


This meeting is part of Management Forum's 30th Anniversary Congress and will enable delegates to understand the qualifications and role being proposed for the Qualified Person for the medical device manufacturer.

Organiser: Management Forum

Featured Companies

Related Content

Medical Device Regulations in the Middle East
Medical Device Regulations in the Middle East
Biological Evaluation of Medical Devices
Biological Evaluation of Medical Devices
Medical Device Summer School: From concept to CE marking
Medical Device Summer School: From concept to CE marking
Pre-filled Syringes - Advances in Manufacture
Pre-filled Syringes - Advances in Manufacture
Device/Drug and Drug/Device Combinations in the EU and USA
Device/Drug and Drug/Device Combinations in the EU and USA
Usability and human factors engineering
Usability and human factors engineering
Injectable Drug Delivery
Injectable Drug Delivery
Design, development and performance evaluation of medical devices
Design, development and performance evaluation of medical devices
FDA Medical Device Inspections
FDA Medical Device Inspections