1:04:05
Q2 2026 Medical Device Regulatory Update: FDA QMSR, EU MDR, AI Review & Cybersecurity
NSF
1:04:11
International Medical Device Registration Explained: Global Strategy, Challenges, and Market Entry
45:13
FDA Medical Device Market Entry: 510(k), De Novo, and PMA Explained for Life Sciences Leaders
1:25:01
ISO 10993-1:2025 Explained: What Medical Device Teams Need to Change in Biological Evaluation
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Medical Device Risk Management Under ISO 14971, MDR, and IVDR: A Practical Guide for Manufacturers
48:36
Post-Market Surveillance for Medical Devices: EU, UK, FDA, and Canada Explained
47:09
FDA QMSR Is Here: What ISO 13485 Alignment Means for Medical Device Quality Systems
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Electronic IFU for Medical Devices: EU MDR Requirements, Risk Assessment, and Implementation Steps
42:28
AI-Enabled Medical Devices: Managing Model and Data Lifecycle Risk in Regulated Environments
0:34
What Regulators Expect From QMS Leadership
0:37
What Internal Reviews Often Miss
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NSF Webinar on the Life Science Sector in Ireland: Promo
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Changing Requirements for Manufacturers Under IVDR
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Why Work at NSF?
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Enrichment Strategies to Increase the Power Reduce the Sample Size in Clinical Trials
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Seminário On-line: Requisitos Internacionais para Fabricantes de IVD
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Regulatory Q&A Session With NSF Experts
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Adopting Digital Solutions in the Medical Device Industry
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Are You Prepared for MDR/IVDR?
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Webinar: A Regulatory Q&A With IVD Expert Robyn Meurant
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EU MDR Training by NSF International
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NSF's Remediation Resources
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Reopening your business and the use of face masks
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Emergency Market Authorization for COVID-19 IVDs. Emergency Use Authorization (EUA)
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Upgrading the FDA Adverse Event Reporting Systems - FAERS
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Webinar: Clinical Investigations - Transitioning from MDD to MDR
50:28
Clinical Evidence for Medical Devices Under Regulation (EU) 2017/745
1:21
How to meet new European Reg. Requirements for IVDs
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How to Deal With the New Post-Market Surveillance Requirements Under Regulation (EU) 2017/745
39:39
Clinical Evidence for Medical Devices
International Standard for Medical Device Quality Management Systems
Medical Device Complaint Handling
In Vitro Diagnostic Device Regulation (IVDR)
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Implementing a Simplification Strategy | NSF International
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How to prepare for EU MDR
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The New EU MDR PMS Requirements Webinar
LIVE
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Medical Device Regulation Training - MDSAP Training
1:03:12
How to prepare for the changes to OEM medical devices under the new MDR
35:15
In Vitro Diagnostic Regulation - IVDR
42:39
Future of Clinical Data and Medical Device Regulation 2017/745
28:51
MDSAP - Medical Devices Single Audit Program Training
7:03
NSF Medical Devices Services
