Medical Device 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.
Learn more about our quality management systems and GMP training. Whatever your requirements, our expert team has you covered.
View upcoming and online courses
Available Training Types
- Online
- Virtual Learning
Need Corporate In-House Training?
We can deliver our broad range of courses in a format and time frame that works for you and your team.
Instructor-Led Courses
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ISO 14971:2019 - Risk Management for Medical Devices and IVDs - Practical Application
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ISO 13485-2016 - Fundamentals -Medical Devices - QMS - Requirements for Regulatory Purposes
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Preparing for FDA Medical Device Inspections – Practical Guidance
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Preparing for FDA Medical Device Inspections – The Requirements
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ISO 19011-2018 - Applying Principles to Medical Device QMS Audits
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ISO 9001:2015 – An Overview and Changes
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CAPA Considerations: Problem Statement Writing and Investigation Techniques
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Writing Effective Nonconformity Statements During Medical Device QMS Audits
Online Self-Paced Courses
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Post-Market Surveillance and Vigilance Requirements for Manufacturers (EU 2017/745)
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U.S. Medical Device Quality System & Combination Products Regulations – Practical Instruction
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U.S. FDA Medical Device Reporting Requirements
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Medical Device Complaint Handling and Servicing
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ISO 14971:2019 - Application of Risk Management to Medical Devices Overview
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ISO 13485: Medical Devices QMS - Requirements for Regulatory Purposes
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ISO 17025 General Requirements for Testing and Calibration Laboratories
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Introduction to Writing Effective Nonconformity Statements During Medical Device Manufacturer QMS Audits
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FDA Inspections of Medical Device Manufacturers
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Understanding Top Management Responsibilities for Medical Device Quality Management Systems