Join Cormica's Biocompatibility Webinar: Expert Insights on ISO 10993 & Regulatory Compliance
Wickham Micro is excited to share an upcoming webinar from Cormica, covering essential insights into biocompatibility testing for medical devices. This expert-led session will explore ISO 10993 requirements, key differences in FDA and MDR submissions, and strategies for ensuring regulatory compliance.
Key Takeaways From The Webinar:
- Understanding ISO 10993 and its role in regulatory compliance
- Key differences in biocompatibility requirements for FDA and MDR submissions
- How to develop a tailored biocompatibility testing strategy to streamline approvals
- Case studies demonstrating successful approaches to biological safety evaluation
Perfect for professionals in medical device development, regulatory affairs, and quality assurance, this webinar provides practical guidance on streamlining biocompatibility assessments and navigating global regulatory landscapes.
