Main Conference Day 3
Wednesday, March 1st, 2017
2:00 PM The Impact of the 2020 MDR on Biological Evaluation of Medical Devices, Including the Role of Extractables and Leachables in Biological Risk Assessment
• Identify what is meant by biological safety and overview the relevant guidance documents
• Discuss the parts of the MDR which relate to biological safety
• Will the MDR requirements have an effect on biological safety evaluation going forward?