Dental Product Testing & Safety: Bridging Science, Risk & Regulation

Join us for an immersive, full-day workshop exploring the regulatory requirements and practical implementation of biocompatibility testing, risk evaluation, and packaging validation for dental medical devices.
This on-site workshop combines standards-driven knowledge with real-world case studies, helping participants confidently navigate the complex testing landscape.

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📅 Date: 7th July 2026
🕘 Time: 9:00 – 16:45
📍 Location: Eurofins BioPharma Services Consulting Munich GmbH, Robert-Koch-Straße 3a, 82152 Planegg/Munich, Germany
💬 Language: German
💶 Partecipation fee: €250

Who should attend?

• Dental medical device development
• Material and product testing
• Regulatory submissions and compliance

It is especially relevant for professionals in:

• Quality Assurance (QA)
• Regulatory Affairs (RA)
• R&D and product development
• Testing and laboratory teams

Participants will gain practical, immediately applicable insights to support compliant development and approval of dental devices.

Developing and testing dental medical devices requires navigating stringent biocompatibility and packaging regulations, particularly under ISO 10993, ISO 7405, and ISO 11607. This workshop is designed to provide practical, science-based, and audit-ready guidance for manufacturers and developers.

Through expert-led sessions and real-world examples, participants will:

✅ Gain clarity on biological evaluation requirements, including:

• ISO 10993-1 updates and implications
• ISO 7405 specific requirements for dental products
• Risk-based test selection strategies

✅ Understand material and testing challenges, such as:

• Chemical characterisation (ISO 10993-18)
• Sample preparation for different material types
• Evaluation of biological risks and hazardous substances

✅ Learn from real-world case studies

• Practical implementation of testing strategies
• Transition from theoretical requirements to laboratory execution

✅ Explore advanced topics

• Nanoparticles in dental materials: risks and regulatory expectations
• Testing strategies and documentation approaches

✅ Master packaging validation and shelf-life considerations

• ISO 11607 requirements for sterile packaging
• Packaging methods, sterilisation approaches, and lifecycle considerations

What makes this workshop unique?

• Hands-on learning approach – from test strategy to execution
• Lab tour experience – insight into real testing environments
• End-to-end perspective – from risk assessment to validation
  
  Participants will be guided through:

• Biological evaluation strategy design
• Sample preparation and testing execution
• Interpretation of test results
• Packaging validation and shelf-life assessment