NSF International provides international quality and regulatory training courses to the medical devices industry. We offer public training classes and private in-house courses. Our industry and regulatory experts work with you to deliver flexible, modular and professionally accredited training. Our courses include:
- 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
Our industry and regulatory experts work with you to deliver flexible, modular and professionally accredited training. Our courses include:
• ISO 13485:2016 – Medical Device Quality Management System Requirements
• Medical Device Single Audit Program (MDSAP)
• Medical Device Lead Auditor Training, based on ISO 13485 and MDSAP requirements
• EU Medical Device Regulation and In Vitro Diagnostics Regulation – New Requirements
We offer many training options to meet your particular learning needs. We offer face-to-face classroom training as well as the flexibility of self-paced online learning options.
For more information about NSF Medical Devices training and education, please email firstname.lastname@example.org .