Join us for an informative webinar where we dive deep into the world of biological evaluation of medical devices using the international standard ISO 10993-1. This standard, titled "Biological evaluation of medical devices - Part 1: Evaluation and testing within a risk management process," is a crucial guideline for ensuring the safety and efficacy of medical devices in the global market.

Key Highlights:

• Understanding ISO 10993-1:  Gain insights into the fundamental principles and scope of ISO 10993-1 and why it is essential for the medical device industry.
• Biocompatibility Assessment:  Learn how to conduct biocompatibility assessments for your medical devices by ISO 10993-1.
• Risk Management:  Explore the integration of ISO 10993-1 within your risk management process, ensuring compliance and safety.
• Case Studies:  Dive into real-world case studies showcasing successful implementation and compliance with ISO 10993-1.
• Q&A Session:  Engage with our expert panel in a live Q&A session to get answers to your specific questions.

Why Attend?

• Learn about the latest requirements for ISO 10993-1 compliance
• Get expert advice on how to implement ISO 10993-1 in your organization
• Ask questions and get answers from experienced professionals

Who Should Attend?

• Regulatory Affairs Professionals
• Quality Assurance Specialists
• Biomedical Engineers
• Product Development Teams
• Medical Device Manufacturers
• Anyone involved in the medical device industry