An NSF International Company

Check out our Training Course Schedule

Choose your country and register for a training event today

Risk management in design for medical devices; Implementing ISO 14971

Print

Part of medical device design, development and product validation (module 2) - attend one or all of the sessions.

Dates: Thursday 24 to Friday 25 October 2025
Venue:
AMP Technology Centre, Sheffield, UK
Cost:

£1200.00 excl. VAT - £1440.00 inc VAT

Type: Medical Devices

About this course

ISO 14971 is the standard adopted by the medical device industry for demonstrating that the clinical benefit of a device outweighs all technological and user related risks. ISO 14971 requires risks to be identified, controlled and evaluated with respect to the entire product lifecycle and, as such, requires the implementation of formal, structured risk management activities and processes throughout the organisation.

We concentrate upon the application of risk management within the design of medical device products, ultimately enabling you to demonstrate that you have adopted the necessary controls to achieve product safety and efficacy.

This course will provide you with the technical knowledge to adopt and implement risk management within your development organisation; to cover the diverse activities of design, validation, manufacture, use, service and disposal of your devices.

The course is designed to give you the knowledge and skills necessary to implement risk management in sufficient technical detail to be able to present your risk management activities with confidence to International regulatory agencies, not least European competent authorities and notified bodies as a basis for market approval.

Who Should Attend

  • Design engineers
  • QARA professionals
  • Consultants wishing to advise organisations on risk management
  • Notified body auditors and reviewers
  • Competent authority personnel wishing to understand the practical application of risk management
  • Risk management and safety managers
  • Pharmaceutical Qualified Persons with responsibility for medical devices
  • Pharmaceutical Qualified Persons wishing to transfer to the medical device industry

Quick links

NSF-DBA have offices in Kirkbymoorside and Sheffield, UK and Boston and Ann Arbor, USA

A word from NSF-DBA

If you do not find the course you are looking for please contact me at the NSF-DBA Kirkbymooorside Office

Bev Willett, Course Administrator, NSF-DBA

© NSF-DBA 2013

Registered Office: NSF-DBA, The Georgian House, 22/24 West End, Kirkbymoorside, York, UK, YO62 6AF
Registered in England and Wales No: 3432550 | Tel: +44(0)1751 432999 | Fax: +44(0)1751 432450 | Email: [email protected]
US Office: NSF-DBA LLC, 6th floor, 129 South St, Boston, MA 02111 | Tel: 1-857-277-0060 | Fax: 1-857-284-7207 | Email: [email protected]