
3rd Annual European Medical Device Biocompatibility Conference
- 23rd & 24th September 2025
- Virtual Conference
We Interact Together Innovate Together Inspire Together
Biocompatibility Excellence: Insights, Innovations, and Impact
Key Areas of Discussion and Outcomes from This Conference:
- Best Approach to Chemical Characterization, Biological Evaluation, Toxicological Risk Assessment as per ISO 10993-17:2023
- Impact of Degradable, Absorbable, and Resorbable Materials on Biocompatibility and Biological Response
- Evolving Requirements for Biological Equivalence Under EU MDR, Including Distinctions from MDD
- Best Practice In Interpreting E&L and AET Data for Safety Assessments, Strategies for Combination Products
- Navigating Audit Challenges and Best Practices for Submission Alignment (BEP, TRA, BER), and 2024 Compliance Updates
- Addressing Global Trends from In Vivo To In Vitro Testing, In Vitro Modelling, Use of AI and Organ-On-A-Chip Technologies to Reduce Animal Testing
- Mitigating Regulatory Hurdles and Harmonizing FDA ISO 10993-1, and EU MDR Testing Standards
- Case Study Insights on Irritation Testing Variability and Evaluation of Blood-Contacting Devices
- Best Practices for TPL Partnerships, Ensuring Data Integrity, and Managing Reprocessing Risks for Reusable Medical Devices
Why Attend a TT Conference
- 40+ Professionals from the Medical Device Biocompatibility Department only!
- 10+ Solution-Focused Sessions
- Exclusive Networking Opportunities
- A Limited Number of Attendees
Maximum Engagement
- 04 Roundtable Discussions
- 02 Days of Knowledge Sharing
- 01 Panel Discussion
- 01 Fireside Chat
Top Speakers

Dujuan Lu
Manager/Global Lead | Extractable and Leachable (E&L) Testing
SGS

Dmitriy Pastarnak
Director, Quality Assurance
EDWARDS LIFESCIENCES

Dr Andreas Nixdorf
Manager - Extractables & Leachables Testing
SGS

Paul Buxton
Director, Biological Evaluation
GEISTLICH PHARMA AG

Alina Martirosyan, PhD, DABT, ERT
Scientific Manager, Toxicology
B. BRAUN

Emilienne Zuyderhoff
Senior Research Associate - EU MDR Biocompatibility
BAXTER
Targeted Content
With our targeted attendee and speaker line-up, you can have meaningful conversations with industry-specific experts who have faced the same situations and challenges. Spark new ideas by brainstorming during our breakout sessions, informal post-session Q&As, panel debates, case studies, and workshops.
Meet Industry Leaders
Our robust screening process ensures an exclusive environment where you can focus on connecting and fostering stronger working relationships with those in the medical device field. Collaborate to find the necessary solutions to your current problems.
Customize Your Content
Get the most out of this event experience by choosing what content is most relevant for you and your company and tailoring your event experience around this decision. Learn and connect with whomever you want, whenever you want, and however you want.