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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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Explore Our Courses

Country-Specific Regulatory Training
Marketing a medical device in a global environment offers many challenges, as regulatory requirements vary widely from one country to another.
Market Access Regulatory Training
Understanding the legal and regulatory framework for developing, marketing and distributing medical devices can be challenging.
Auditor Training
Today’s medical device auditor needs auditing skills, technical skills and up-to-date knowledge of the latest regulatory requirements. Meet these needs with NSF.
QMS and GMP Training
NSF’s training courses give you 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.

Explore Our Courses by Delivery Type

Self-Paced eLearning
Explore and learn at your own pace with self-paced eLearning — a flexible and convenient way to enhance your skills.
Corporate In-House Training
Help maintain and improve compliance, further your team’s professional development and gain a competitive advantage with off-the-shelf and customized in-house training courses.

Interested in Training Your Team?

Find more information about our corporate in-house training services and read client reviews.
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Featured Medical Devices Training

Preparing for FDA Medical Device Inspections – Practical Guidance
Recognizing what to expect during an FDA inspection enables a medical device manufacturer to effectively prepare for the inspection.
CQI/IRCA-Certified QMS Lead Auditor Based on ISO 13485:2016 and MDSAP Requirements
Learners will plan, conduct, report and follow up on a QMS audit in accordance with ISO 13485:2016, MDSAP.
Understanding Top Management Responsibilities for Medical Device Quality Management Systems
Medical device regulators from around the world have recognized the importance of top management’s commitment to quality as essential to establishing and maintaining an effective quality management system.
  • 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

Special Features

Key FDA Policies, Procedures and Practices Before, During and After Medical Device Manufacturer Inspections
Article
This paper 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.
White Paper: Tools and Tips for Writing Effective Nonconformity Statements During Quality Management System Audits of Medical Device Manufacturers
Article
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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