Unlocking Success with ISO 10993-1: Biological Evaluation of Medical Devices

John E. Lincoln
Recording Webinar Available @All Days
Recorded Webinar


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

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