Online Keynotes: Expert-Led Webinars on Medical Device and IVD Compliance
These free-of-charge webinars (keynotes) examine regulatory, quality, and technical issues affecting medical device and IVD manufacturers. They go beyond theory, providing practical strategies, effective compliance approaches, and tools used in real-world regulatory and quality practice.
Attend the live sessions with Q&A or access recordings of past sessions, available to watch at any time.
Upcoming live sessions
Clinical Evaluation for Medical Devices
November 3, 2026
Regulatory Update Q4
December 8, 2026
Combination Products: The 2026 Perspective Navigating Regulatory Change Through an Integrated Lifecycle Approach
December 15, 2026
Past session recordings
FDA QMSR Enforcement: What Recent Inspection Findings Are Revealing
October 15, 2026
Quality Management according to ISO 13485
October 6, 2026
Biocompatibility and Biological Safety of Medical Devices
September 30, 2026
Combination Products in Europe: Navigating Pharma, Devices, and MDR Expectations
September 25, 2026
Regulatory Update Q3
September 15, 2026
Technical Documentation for Medical Devices
August 25, 2026
Regulatory Update Q2
June 16, 2026
International Medical Device Registration: Challenges and Opportunities Across All Continents
June 10, 2026
Market Authorization for Medical Devices in the USA
May 19, 2026
Management of AI-Enabled Medical Devices
April 21, 2026
Regulatory Update Q1
March 24, 2026
Biological evaluation according to ISO 10993-1:2025
February 27, 2026
Risk Management for Medical Devices
February 17, 2026
Post-market Surveillance for Medical Devices
January 27, 2026
From Paper to Digital: Understanding New EU Rules on Electronic Instructions for Use
October 29, 2025
How NSF Can Help You
Get in touch to find out how we can help you and your business thrive.
