Our medical device educational courses are highly interactive and based on real scenarios.
Learn in your preferred format:
Courses cover the following topics:
Quality Management Systems and Good Manufacturing Practices
Get the tools to ensure your product complies with international standards and regulations. Our diverse training programs teach you how to implement and apply global guidelines through all stages of the product lifecycle.
Courses include U.S. quality systems and combination products, risk management, CAPA deviation and inspection readiness courses.
Country-Specific Regulatory Training
Bringing a product to market in multiple countries requires understanding regional differences and complying with all regulations. Our training offering includes ISO standards courses.
Courses cover the United States, Canada, Brazil, Japan, China and Australia, and the European Union Medical Device Regulation (EU MDR) and European Union In Vitro Diagnostic Device Regulation (EU IVDR).
Market Access Regulatory Training
Understanding the legal and regulatory framework for developing, marketing and distributing medical devices can be challenging. Covering everything from how the U.S. Food and Drug Administration (FDA) classifies medical devices to preparing technical files, our experts are here to help.
Auditor Training for Medical Devices
Today’s medical device auditor needs auditing skills, technical skills and up-to-date knowledge of the latest regulatory requirements. Meet these needs with our interactive courses.
Courses cover internal auditor training for the EU MDR, EU IVDR, MDSAP, and a popular CQI and IRCA Certified Lead Auditor Program.
In-House Training for Medical Device Manufacturers
We can bring our medical device courses in-house and deliver to your team to address your unique requirements. NSF’s medical device experts will work with you to recommend the right course from our catalogue — or develop anything from a single session to a multi-component program.