2nd Annual Biocompatibility Testing In Medical Devices 2025 Conference

Place: Porto, Portugal

Date: 06th-07th 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

Featured Speaker Companies:

Exhibition Sponsors

Welcome to the 2nd Annual Biocompatibility Testing in Medical Devices 2025 Conference, which will take place in beautiful Porto, Portugal. We’re thrilled to reunite with esteemed professionals whose contributions have made our past events memorable, and we extend a warm welcome to new participants! Over the two days, prepare to engage in exhilarating discussions, explore groundbreaking solutions, and seize invaluable networking opportunities. Let’s collaboratively propel the future of medical device safety and efficacy forward!

The conference contains

70+ attendees

15+ different topics

Certificate of Participation

8+ 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 2nd Annual Biocompatibility Testing in Medical Devices 2025 Conference

Welcome to the 2nd Annual Biocompatibility Testing in Medical Devices 2025 Conference in the captivating city of Porto, Portugal! We are delighted to welcome back esteemed professionals and extend a warm greeting to new participants joining us this year. Over the two days, engage deeply with pivotal discussions and advancements shaping the landscape of medical device safety and efficacy. The conference will address pressing regulatory challenges, including navigating compliance with ISO 10993 standards and understanding the impact of extractables and leachables in medical devices. Attendees will gain insights into cutting-edge biocompatibility testing methods, comparing in vitro and in vivo approaches, and practical considerations when collaborating with third-party laboratories. Moreover, sessions will delve into the latest updates under EU MDR, focusing on biological equivalence and effective post-market surveillance strategies. Global harmonization efforts and their implications for biocompatibility standards will also be explored. Join us in driving innovation and setting new benchmarks to ensure the highest standards of safety and effectiveness for medical devices worldwide. We look forward to productive discussions, valuable networking opportunities, and collectively shaping the future of biocompatibility testing!

Discover Porto: The Perfect Conference Destination

Porto, a vibrant city in northern Portugal, stands out as an exceptional destination for hosting conferences. Known for its rich history, stunning architecture, and world-renowned port wine, Porto offers a unique blend of tradition and modernity. The city’s well-equipped conference venues, excellent transport links, and welcoming atmosphere make it an ideal choice for business events.

Attendees can explore the picturesque Ribeira district, enjoy a cruise on the Douro River, and savor exquisite local cuisine. The Alfandega Congress Centre and the historic Palácio da Bolsa provide unique settings for events, blending old-world charm with modern amenities.

Porto’s rich cultural offerings include museums, galleries, and historical sites like São Bento Railway Station and the Sé Cathedral. The city’s vibrant dining scene features local delicacies such as bacalhau and the iconic Francesinha sandwich.

Porto’s charm and dynamic environment ensure an inspiring and memorable experience for all conference participants.

Past Event

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

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