Medical Devices and IVDs Training

NSF provides regulatory and quality medical devices training courses and professional qualifications. Based on timely, real-world experience rooted in industry best practices and regulator insights, NSF’s interactive training helps you meet international requirements throughout the product lifecycle.

Choose from instructor-led and online, self-paced medical devices training courses created by our team of leading global experts, or work with us to incorporate your company’s business operations, policies, procedures, brand and messaging into our training offerings.

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Featured Medical Devices Training

The day was excellent. The technical content and relevance were very good.
Simon Redfern
Smiths Medical
This course has perfectly provided the learning needed for current projects at work.
Wolfgang Angermann
Stryker, Ireland
Great course; challenging with nowhere to hide in the background and plenty of chances to ask general questions.
Peter Iddon
Neotherix

Medical Devices and IVDs Training

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Country-Specific Regulatory Training

Market Access Regulatory Training

Auditor Training

QMS and GMP Training

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Self-Paced eLearning

Corporate In-House Training

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Featured Medical Devices Training

Preparing for FDA Medical Device Inspections – Practical Guidance

QMS Lead Auditor Based on ISO 13485:2016 and MDSAP Requirements

Understanding Top Management Responsibilities for Medical Device Quality Management Systems

Special Features

Key FDA Policies, Procedures and Practices Before, During and After Medical Device Manufacturer Inspections

Two of the Most Common IVDR Challenges (With Solutions)

White Paper: Tools and Tips for Writing Effective Nonconformity Statements During Quality Management System Audits of Medical Device Manufacturers

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