2nd Annual Medical Device Biocompatibility Conference

Future Event • 21st November 2024 • 22nd November 2024 • Berlin, Germany

We are delighted to invite you to our upcoming “2nd Annual Medical Device Biocompatibility Conference" set to take place on the 21st – 22nd November 2024 in Berlin Germany!

Upcoming conference will gather in Berlin up to 100 high-level executives from the top companies in the world. Closed-door business conference will be packed with pre-event get together meeting: tie-off atmosphere for all our participants with a great opportunity to meet exhibition and sponsorship partners and have a face to face productive networking with all other experts and professionals from the industry prior the main presentations.

Conference will include 20+ innovative presentation sessions from well-known and highly experienced speaking partners and cover a wide spectrum of topics: starting from the regulatory updates, the latest innovations in the industry, technological research, modern manufacturing processes and trends in medical devices biocompatibility market which can help to all participants with current and future challenges and to show how to develop the proactive approach.

Do not miss the chance to meet high-level representatives and have a clear vision of the profound transformations to come, made possible by the massive growth of the innovative medical device industry nowadays.

We look forward to welcoming you and your colleagues to the conference on the 21st – 22nd November 2024 in Berlin Germany.

Who Should Attend:

This conference will gather together: CEOs, CTOs, CIOs, COOs, SVPs, VPs, Directors, Global Heads, Heads, Managers, Team Leaders, Specialists, Strategists, Planners and Officers of the following divisions:

  • Toxicology
  • Medical Device
  • Biocompatibility
  • Analytical Chemistry
  • Research and Development
  • Safety and Risk Assessments

  • Materials Science and Selection
  • Product and Process Development
  • Marketing and Business Development
  • Manufacturing Science and Technology
  • Quality Assurance and Regulatory Affairs

Key Practical Points:

  • Regulation and legislation updates
  • Biocompatibility Challenges and Solutions
  • Understanding ISO 10993-1 and ISO 10993-18 for regulatory compliance
  • Crafting effective biological evaluation plans and connecting them to overall safety
  • Exploring novel approaches for extractable/leachable assessment
  • Managing risks through effective toxicological assessments
  • Identifying common problems and optimizing biocompatibility testing
  • Implementing alternative approaches in biocompatibility testing
  • Evaluating nanomaterials and understanding their implications
  • Harnessing the power of in vitro methods for cytotoxicity testing
  • Utilizing reconstructed human epidermis assay for irritation testing.
  • Staying updated on advancements in sensitization testing
  • Navigating ADME requirements under MDR and assessing CMR/ED substances
  • Conducting degradation testing and evaluating its significance
  • Opportunities for hands-on exercises, working groups, and case studies
  • Business networking lunches and optional tour and dinner for informal interactions
  • Gaining insights into regulatory frameworks and compliance requirements
  • Understanding the legal and regulatory consequences of biocompatibility failures

Benefits for Our Attendees:

  • By attending our business conference you will get an access to a new solutions for your business development
  • Conduct face to face business meeting with experts and professionals to discuss current and future challenges and develop the proactive approach
  • You will have an opportunity to interact and discuss about industry challenges and keynote speaker presentations during Q&A sessions right after each presentation
  • Make a business contact with a top leader experts and solution providers to solve most of business challenges
  • You will get full access to all event’s presentations and conference materials