Biological Evaluation of Medical Devices is a conference that covers topics such as:
- Hazardous situations
- General principles of biological risk management
- Materials characterisation
- Reviewing existing data
- Quantitative toxicological risk assessment (QTRA)
- Evaluating chemical data
- Risk assessment and control
- Biological testing
- Risk review
Biological Evaluation of Medical Devices brings together:
- R&D
- Regulatory affairs
- Analytical chemistry
- Product safety/toxicology
- Materials research and evaluation
- Risk assessment and risk management
- Regulatory Authorities, Notified Bodies and CROs regulating or supporting the medical device industry
