Biological Evaluation of Medical Devices

Topics

• 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

Who should Attend

• 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