Biological Evaluation Under ISO 10993-1:2025 - Live Q&A
This webinar examines the changes introduced in ISO 10993-1:2025 and explains what they mean in practice for medical device manufacturers.
Nächster Termin20.02.2026
Start / Ende16:00 / 16:45
OrtOnline
Kostenab 0,00 €
Beschreibung
Biological Evaluation Under ISO 10993-1:2025 - Live Q&A
The 2025 revision of ISO 10993-1 introduces substantive changes to the biological evaluation of medical devices, strengthening alignment with risk management principles and providing updated guidance on device characterization, exposure duration, and the identification of biological effects. Biological evaluation remains a core element of medical device conformity assessment.
In this session, you will learn:
Key updates in ISO 10993-1:2025 and their practical implications
How biological evaluation integrates into the risk management process
When a short-term update to an existing biological evaluation is required
Bring your questions as this keynote will be followed by a Live Q&A.
Who should attend
This webinar is intended for quality, regulatory, and medical device professionals involved in biological evaluation, risk management, and conformity assessment.
Register to understand the impact of ISO 10993-1:2025 and how to apply the updated requirements effectively.
If you can’t make the date, we’ll send you the on-demand recording
