Training

Risk Management for Medical Devices 

Training Methods: Virtual Training ○ On-Site ○ Bespoke

Course Overview

Our industry leading experts have created a 2-day course to help you understand the requirements of ISO 14971 and the importance for medical device manufactures.

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This course explores the ISO 14971 standard clause by clause to ensure a thorough understanding of the requirements. During this course you will also be provided an understanding of how ISO 14971 aligns with the new MDR and IVDR regulations.

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This course is fully interactive and offers you the chance to take part in group activities, participate in polls and share and download course materials. 

We are here to help you make your medical devices compliant.

At A Glance

- 2-days of fully interactive training

- Instructor-led virtual classroom

- PDF Certificate of completion

- Live Q&A sessions

- PDF Copies of the slides, handouts and templates

- Bespoke and on-site training available 

Who Should Attend?

This training course is recommended for anyone involved in risk management.

- Regulatory Affairs Professionals

- Research and Design Engineers

- Quality Managers

- Quality Engineers

- Manufacturing Engineers

- Internal Auditors

- Marketing

- Clinicians

"Thoroughly enjoyed the 2 day course! Rod was very insightful and knowledgeable. It was a great experience, that I would highly recommend to any medical professional." 

Ash P

RB

"The course was very comprehensive considering how large the topic is. I learnt a lot more than I expected to and the knowledge of the lecturer was excellent with a lot of hands on experience and advice." 

Angela H

Sysmex

"Rod is a great communicator and set up a really good course. You could feel his passion for the field and his vast hands-on experience. I would definitely recommend this course to anyone."

Malene L

Coloplast