Medical Device Training and Education

NSF Health Sciences Medical Devices provides international quality and regulatory training courses, as well as professional qualifications.  These courses are delivered both at our location and yours.  Module topics include understanding the U.S. FDA 510K, PMA, IDE and European CE marking (93/42/EEC, 90/385/EEC and 98/79/EEC), medical device risk management (ISO 14971), and design control and quality system implementation (21 CFR Part 820 and ISO 13485).

Our regulatory science courses cover medical device clinical evaluation (ISO 14155) and biological evaluation (ISO 10993) with popular courses such as Post-Market Surveillance and Medical Device Lead Auditor.

NSF offers flexible, modular and professionally accredited training delivered by industry experts. We provide:

  • Company-wide quality and regulatory awareness modules for U.S. and CE marking
  • Professional certificates and post-graduate qualifications in quality assurance and regulatory affairs
  • Custom training
  • Flexible program of modular-based training courses delivered at our site or yours leading to end-of-module certification
  • Global footprint with local resources in the U.S., Europe and Asia
  • Professional development for quality and regulatory professionals
  • Auditing and inspection training
  • Study days enabling you to upgrade your knowledge by listening to the most experienced people in public health policy, medical device law, medical device science, quality assurance and regulatory affairs   

For more information about NSF Medical Devices training and education and to see a list of courses visit our training section.

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