How to handle the nanomaterials requirements of EU Medical Device Regulation.
OTTAWA, ON, Aug. 17, 2020 /PRNewswire/ – On August 26 2020, Claigan Environmental Inc. (www.claigan.com) will present a webinar on common practices to manage the nanomaterials requirements of the EU Medical Device Regulation (MDR). Unbeknownst to most medical device manufacturers, their product normally contains ingredients that meet the definition of a nanomaterial. This webinar will focus on the definition of nanomaterials, the requirements under EU MDR, common nanomaterials in medical devices, and common practices for EU MDR compliance for nanomaterials in medical devices. As nanomaterials become