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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.

Download our PDF guide to view all our training courses in one place.

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Available Training Types

Online
Virtual Learning

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Featured Medical Devices Training

Online

Understanding Top Management Responsibilities for Medical Device Quality Management Systems

This course is designed to efficiently focus on top management obligations relative to FDA’s Quality System Regulation and ISO 13485:2016. This course does not simply focus on the requirements of...

Virtual Learning

CQI & IRCA-certified QMS Lead Auditor based on ISO 13485:2016 and MDSAP Requirements

May 8 – 12, 2023

This course consists of five days of instruction followed by a comprehensive written (two-hour exam) on the sixth business day. Learners will plan, conduct, report, and follow up on a...

Virtual Learning

FDA Medical Device Inspections: What to Expect

May 17 – 18, 2023

Understanding what to expect during an FDA inspection enables a medical device manufacturer to prepare effectively for the inspection. This course focuses on identifying FDA inspection criteria, resources (including key...

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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

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Special Features

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

This paper by expert Rob Ruff provides a behind-the-scenes look at how FDA medical device inspections are planned, conducted and managed.

Two of the Most Common IVDR Challenges (With Solutions)

Learn more about two of the most common challenges for IVD manufacturers in meeting IVDR compliance: performance evaluation and post-market requirements.

Insights and Expertise

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

As a medical device quality management system auditor, one of the most important (if not the most important) responsibilities of your role is to effectively communicate identified nonconformities to the auditee organization.

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