Public Events - Medical Devices Training

With a unique approach to expert-led medical devices training and education, NSF International's philosophy is “learning through doing with experts at your side.” Our public events ensure that the key quality assurance and regulatory affairs (QA/RA) training requirements of your business are met, while introducing the latest QA/RA intelligence, techniques and tools. They are highly interactive and walk students through real problems and scenarios found in the medical device industry. NSF’s team of highly qualified and internationally acclaimed regulatory affairs and quality affairs experts helps professionals stay up to date on issues affecting the medical device industry.

NSF offers top quality public courses on a vast range of topics such as ISO 13485:2016 training, Medical Device Single Audit Program (MDSAP) training and a CQI/IRCA accredited ISO 13485 Lead Auditor training for medical devices course that incorporates ISO 13485:2016 and MDSAP components. Course duration ranges from one to five days depending on the complexity of the topic, the degree of detail covered and whether there is a need for an end-of-course examination to support qualification or certification schemes.

Check out our upcoming medical devices training courses and webinars below to learn more!

Upcoming Courses & Webinars

In Public Events - Medical Devices Training
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