Join global leaders in biocompatibility toxicology regulatory science and medical device innovation for a high-level two-day summit in the heart of Europe.
The Medical Device Biocompatibility & Safety Summit 2025 will deliver cutting-edge insights on ISO 10993 MDR FDA risk management testing and safety innovation — all while offering real-world guidance and networking with top stakeholders.
🎯 Why Attend?
- In-depth discussions on ISO 10993 MDR and FDA regulations
- Practical guidance on toxicological risk assessment & biological evaluation
- Expert-led sessions with case studies and live panels
- Strategic networking with RA/QA R&D CROs and manufacturers
- Explore the future of medical device safety compliance and innovation
👥 Who Should Attend:
- Regulatory Affairs & Quality Assurance Professionals
- R&D and Toxicology Scientists
- Biocompatibility & Clinical Evaluation Experts
- Medical Device Manufacturers
- CROs Testing Labs and Consultants
- Compliance Officers & Risk Managers
🎟️ Early Bird Offer:
Request early-bird registration access and group discounts by contacting:
#MedicalDevices #Biocompatibility #MedTech #MedicalDeviceSafety #RegulatoryAffairs #ISO10993 #Toxicology #FDACompliance #MDR #RiskManagement #HealthcareInnovation #MedTechSummit #MedicalConference #Prague2025 #GrandiumPrague #monbienevents
Event Venue
Grandium Hotel Prague, Politických vězňů 913/12, Nové Město, 110 00 Praha-Praha 1, Tchéquie, Prague, Czech Republic
USD 1299.00 to USD 1999.00
