12th - 13th October 2021 | Germany
Sophie Clewlow, Higher Medical Device Specialist at MHRA

Sophie Clewlow

Higher Medical Device Specialist

Check out the incredible speaker line-up to see who will be joining Sophie.

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Day 3 - Future Technology

Thursday, February 20th, 2020

1:50 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?