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2nd Annual Biocompatibility Testing, Material Safety & Contaminant Control for Medical Devices 2026 Conference

Place: Budapest, Hungary

Date: 01-02 of October 2026
Language: English

Key points:

  1. Regulatory Compliance Updates
  2. Advanced Biocompatibility Testing Methods
  3. Chemical Characterization & Impurity Control
  4. Risk Assessment & Material Selection
  5. Emerging Trends in Materials & Testing Technologies
  6. Post-Market Surveillance & Lifecycle Monitoring
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Dear Colleagues,

It is with great pleasure that we invite you to the 2nd Annual Biocompatibility Testing, Material Safety & Contaminant Control for Medical Devices 2026 Conference, in Budapest, Hungary.

The conference contains

15+ different topics

Certificate of Participation

10+ hours networking opportunities

Panel discussion

Workshop

Q&A Sessions

Post-conference materials

Our Past Speakers:

Past Exhibition Sponsors

Past Keynote Sponsors

Past Media Partners

The Journal of Medical Device Regulation is a practical tool for every regulatory professional working in the medical device and in vitro diagnostics (IVD) industries. The Journal looks at the impact of future, recent and past regulatory developments for the medical device industry, which is indispensable for the success of your company’s regulatory and commercialisation strategies. The Journal delivers in-depth regulatory affairs review and discussion articles by experts from the medical device community as well as insights from the Competent Authorities and Notified Bodies. The Journal also summarises the regulatory news headlines from around the world on topics vital to the medical device and IVD industries – both pre- and post-market – from classification and registration requirements to clinical investigations, standards and labelling to name but a few.

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.

Discover Budapest: Central Europe’s Cultural and Scientific Hub

We are honored to host the 2nd Annual Biocompatibility Testing, Material Safety & Contaminant Control for Medical Devices 2026 Conference in the beautiful city of Budapest, a European hub renowned for its scientific excellence, innovation, and rich cultural heritage. Often referred to as the “Heart of Europe,” Budapest has a long-standing tradition in medical research, engineering, and regulatory science.

With its excellent international connectivity, modern and convenient infrastructure, Budapest offers a seamless experience for local and global attendees. Beyond the conference, the city’s vibrant cultural scene, stunning architecture, and historic thermal baths, ensure a memorable and enriching experience both professionally and culturally for all participants.

We look forward to welcome you!

What our clients say about our Events

"I had the privilege of speaking at the VNA International Conference on Biocompatibility Testing, Material Safety & Contaminant Control in Medical Devices in Barcelona, Spain, and I highly recommend VNA International for the quality and caliber of its technical conferences. VNA International brings together global medical device leaders and colleagues from across Europe, Central & South America, and the United States, creating a forum for meaningful, high-value dialogue on biomaterials, biocompatibility, toxicology, and patient safety. The program was well curated, technically rigorous, and focused on real-world challenges facing the medical device industry. The conference fostered thoughtful discussion, knowledge exchange, and global collaboration, exactly what is needed to advance patient-centered design and sound regulatory decision-making. I appreciate VNA International’s commitment to connecting experts and elevating the conversation around medical device safety and innovation."
William R. Drummond, Jr. BSc, MBA
William R. Drummond, Jr. BSc, MBA Principal Biomaterials Scientist
“The VNA Biocompatibility Testing and Material Safety Conference 2025 was an exceptional event — expertly curated, deeply informative, and highly relevant to the challenges we face in today’s regulatory landscape. The quality of speakers and technical discussions reflected the best of our industry’s collective expertise. As someone working daily at the intersection of clinical, regulatory, and materials science, I found the sessions particularly valuable for bridging regulatory expectations with practical implementation — from ISO 10993 and 18562 updates to evolving global perspectives on chemical characterization and toxicological risk assessment. VNA Events would be my first choice as an event organizer for future conferences. Their professionalism, attention to detail, and ability to deliver small, high-calibre technical events that foster meaningful exchange are truly unparalleled. It was a pleasure to contribute and to be part of such a well-organized and impactful meeting.”
JACQUELINE VAN DRUTEN (MICR.CIM.RD)
JACQUELINE VAN DRUTEN (MICR.CIM.RD)
"The 2024 Biocompatibility Testing in Medical Devices Conference in Munich was an amazing learning experience. There were many people from all backgrounds in the biocompatibility areas. Munich was a great choice as the city offered all kinds of outside exploring and activities that allowed more networking opportunities to naturally arise. I’m very grateful for being able to attend in person and getting to meet so many amazing people. Thank you for this event, and I hope that I will be able to attend another one someday!"
Cassidy Creemer
Cassidy Creemer
"Thanks for organizing the event, I truly enjoy the 2 days conference!"
Xiaoou Fan
Xiaoou Fan
"I'd like to express my sincere appreciation for the exceptional organization of the conference. The topics discussed were not only captivating but also delved into cutting-edge techniques in the field of 3D cell culture and 3D microscopy. The speakers, true experts in their domains, added immense value to the event. Thank you for such an enriching experience."
Fatemeh Alaei Faradonb
Fatemeh Alaei Faradonb
"I had a great time at the conference!"
Klara Hammarstrand
Klara Hammarstrand
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Biocompatibility Testing, Material Safety & Contaminant Control in Medical Devices 2025 Conference - Barcelona, Spain
September 29th-30th

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