Medical Devices
NSF's range of consulting, training, and auditing services for medical device, IVD and combination product manufacturers are called upon by companies globally. Our ability to navigate the maze of ever-changing regulations enables us to deliver consistent outcomes for client companies.
Mitigate risk, ensure compliance with international and FDA regulations and standards, and apply effective quality systems with expert advice from NSF.
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Use of NSF consulting services or attending NSF training sessions does not provide an advantage, nor is it linked in any way to the granting of certification.
Webinars (Keynotes): Medical Device and IVD Compliance
Free, expert-led online sessions covering regulatory, quality, and technical topics for medical device and IVD manufacturers, with a focus on practical compliance and real-world application. Live Q&A is included, with recordings available to watch at any time.
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NSF Annual Review and Impact Report 2025 Now Live
April 20, 2026NSF has published its Annual Review and Impact Report 2025, detailing the organization’s progress over the past year and outlining strategic priorities for 2026.
European Commission Puts the Delay to EU MDR Transition Timelines to the Vote
January 11, 2023The European Commission published its proposal paper on the transition provisions for medical devices and in vitro diagnostic medical devices on January 6, 2023, it sets out the new transition deadlines and is a must read for the MedTech industry.European Commission Proposes Delay to EU MDR Transition Timelines
December 20, 2022Since the EU MDR came into force in 2017, large parts of the MedTech industry and notified bodies have warned that the capacities of the notified bodies to issue new certificates could become the decisive bottleneck for the implementation of the EU MDR and the EU IVDR. This fear has solidified in the last five years.
Are You a Medical Device and IVD Expert? Join Our Consulting Team!
August 9, 2021We're recruiting! NSF has several open consulting roles across the globe. We would love to chat with you about your experience and discover how you could be an asset to our organization.
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