Part 3: Safety Assessment of Medical Devices

Gain insight into biocompatibility evaluation of drug-device combination products

Safety assessment of drug delivery devices can be a challenge as you must meet the regulatory requirements for both drugs and medical devices for the same product. In this webinar you will get an overview of how to approach safety evaluation of drug delivery devices in accordance with the requirements in the new EU Medical Device Regulation (MDR) and the updated ISO 10993-1 standard (~45 min). Please note that this webinar was recorded in late 2019. Since then the European Commission has postponed implementation of the MDR until 26 May 2021. This does not affect the guidance and relevance of the webinar.

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