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Understand how these updates impact the biological evaluation and compliance of medical devices. The webinar covers:
An overview of the most significant updates to ISO 10993-1.
The regulatory and safety rationale behind the changes.
Anticipated industry challenges and practical ways to address them.
Clarification of new requirements and their implications.
Q&A session to address audience concerns and questions.
Our blogs, insights, webinars and resources will help you understand and stay current on medical device changes, revisions, and insights.
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