3rd Annual Biocompatibility Testing In Medical Devices 2026 Conference

Place: Rome, Italy

Date: 05th-06th of March 2025
Language: English

Key points:

  1. Notified Bodies: Challenges in Regulatory Compliance for Biocompatibility
  2. Regulatory Requirements for Biocompatibility: ISO 10993 Series
  3. Extractables and Leachables (E&L) in Medical Devices
  4. Chemical Characterization and Risk Assessment
  5. Biological Equivalence Under EU MDR
  6. Post-Market Surveillance and Regulatory Compliance
  7. Advances in Biocompatibility Testing Methods: In Vitro vs. In Vivo
  8. Practical Considerations for Testing with Third-Party Laboratories
  9. Global Harmonization of Biocompatibility Standards

Our Previous Speakers:

Our previous sponsors

Dear Colleagues,
It is with great pleasure that we welcome you to the 3rd Annual Biocompatibility Testing in Medical Devices Conference, taking place on March 5-6, 2026, in Rome, Italy.
As the medical device industry continues to evolve, biocompatibility testing remains a critical component in ensuring patient safety and regulatory compliance. With the continuous updates in ISO 10993 standards, the increasing complexity of chemical characterization, and the push towards alternative in vitro methods, it is essential for professionals in the field to stay ahead of the latest developments.
This conference will bring together leading experts, regulatory representatives, and industry pioneers to discuss the latest regulatory updates, advanced testing methodologies, and best practices for ensuring the safety of medical devices. You will have the opportunity to engage in thought-provoking discussions, explore cutting-edge technologies, and network with professionals shaping the future of biocompatibility testing.
We look forward to welcoming you in Rome for an exciting and insightful event.

VNA International team

The conference contains

15+ different topics

Certificate of Participation

10+ hours networking opportunities

Panel discussion

Workshop

Q&A Sessions

Post-conference materials

Expected Speakers from:

  • Medtronic: A global leader in medical technology, Medtronic has extensive experience in biocompatibility testing across a wide range of medical devices.

  • Johnson & Johnson Medical Devices Companies: With a diverse portfolio of medical devices, J&J can provide insights into biocompatibility challenges and solutions.

  • BD (Becton, Dickinson and Company): BD specializes in medical technology and can share expertise in materials selection and regulatory compliance.

  • Abbott Laboratories: Known for innovative medical devices, Abbott can discuss its approaches to biocompatibility and safety testing.

  • Boston Scientific: A leading manufacturer of medical devices, Boston Scientific can offer insights into biocompatibility in the context of cardiovascular and other devices.

  • Siemens Healthineers: As a leader in diagnostic and imaging equipment, Siemens can provide perspectives on biocompatibility considerations for healthcare technology.

  • Philips Healthcare: Philips’ expertise in healthcare technology and equipment makes them a valuable source of knowledge on biocompatibility testing.

  • 3M Healthcare: 3M’s diverse healthcare product range can contribute insights into materials selection and safety assessment.

     

Who should attend:

  • Biomedical Engineers: Join to learn about the latest biocompatibility testing methods and innovations in medical device design.
  • Regulatory Affairs Specialists: Essential to stay updated on regulatory requirements and interact with Notified Bodies for conformity assessments.
  • Medical Device Manufacturers: Gain insights into successful device launches, regulatory compliance, and interactions with Notified Bodies.
  • Quality Assurance Professionals: Learn about standards and best practices validated by Notified Bodies to ensure product quality and compliance.
  • Research Scientists: Attend to explore advancements in biocompatibility research and gather data for Regulatory Affairs submissions.
  • Clinical Research Coordinators: Participate to understand clinical trial requirements and generate data necessary for Notified Bodies’ assessments and Regulatory Affairs submissions.
  • Materials Scientists: Join to discover new materials compliant with regulatory standards and validated by Notified Bodies.
  • Toxicologists: Essential for assessing biocompatibility and safety data required for Regulatory Affairs submissions and Notified Bodies’ evaluations.
  • Notified Bodies: Participate to stay informed about industry advancements and regulatory updates affecting conformity assessment procedures.
  • Regulatory Affairs Managers: Join to coordinate interactions between manufacturers, Notified Bodies, and health authorities to ensure efficient market compliance and product approvals.
  • Students: Engage in tailored sessions focusing on career development, opportunities in biocompatibility testing, and gaining insights from industry leaders.
  • Everyone interested in learning and developing their knowledge and expertise in medical device safety.

Benefits of attendance:

  • Access to Valuable Resources: Gain insights from research papers, case studies, and tools to enrich your projects.
  • Exposure to Cutting-Edge Ideas: Discover innovative approaches and fresh perspectives to refine your strategies.
  • High Networking Opportunities: Engage in extensive networking with experts and colleagues to strengthen connections and foster new relationships.
  • Building Meaningful Connections: Form valuable relationships with peers, industry leaders, and potential mentors.
  • Enhanced Professional Visibility: Elevate your professional presence within your industry and field.
  • Cultural and Global Insights: Gain diverse perspectives and insights into global practices.
  • Enjoy a Memorable Experience: Participate in engaging sessions and activities that create lasting memories.
  • Career Advancement: Obtain a certificate of participation and boost your professional credentials.

About the 3rd Annual Biocompatibility Testing In Medical Devices 2026 Conference

The 3rd Annual Biocompatibility Testing in Medical Devices Conference is designed to address the latest advancements, regulatory changes, and challenges in ensuring the safety of medical devices. As regulatory frameworks such as ISO 10993, EU MDR, and FDA guidelines continue to evolve, manufacturers, toxicologists, notified bodies, and regulatory professionals must adapt to meet compliance requirements and ensure product safety.

This year’s event will focus on:

– The latest regulatory requirements for biocompatibility testing and toxicological risk assessment

– Innovative testing methodologies, including in vitro models, organ-on-a-chip, and AI-driven approaches

– Best practices for extractables & leachables (E&L) analysis and chemical characterization

– Material selection and safety considerations for novel medical device technologies

– Risk-based approaches to cytotoxicity, sensitization, and genotoxicity assessment

Through interactive panel discussions, case study presentations, and hands-on workshops, attendees will gain practical insights into effective strategies for biocompatibility assessment and ensuring compliance with global regulations.
Join us in Rome, Italy, for a conference that will shape the future of biocompatibility testing in medical devices!

Rome: The Eternal City

We are honored to host the ”Global Impurity Control: Nitrosamines, Genotoxicity, and Beyond 2025 Conference in the timeless city of Rome, a place celebrated for its rich cultural heritage and historical significance. Known for its prominence in education and innovation, Rome provides an unparalleled setting to bring together leaders from the pharmaceutical, biotechnology, and regulatory fields. With excellent international access, state-of-the-art venues, and a refined atmosphere, Rome ensures a seamless and enriching conference experience. Beyond the professional opportunities, the city’s vibrant cultural and historical offerings promise a truly unforgettable journey for all attendees.

Past Event

Biocompatibility Testing in Medical Devices Conference
- Munich, Germany
March 21st-22nd 2024

2nd Annual Biocompatibility Testing In Medical Devices 2025 Conference - Porto, Portugal
March 06th-07th 2024

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