QPharma, Inc.'s Medical Device Division Advises Manufacturers to Prepare for UDI Compliance

Published: Aug 22, 2013

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MORRISTOWN, N.J.--(BUSINESS WIRE)--QDevice, the medical device consulting division of QPharma, is advising its clients and all medical device manufacturers to prepare for compliance with the Unique Device Identification (UDI) final rule, which is expected to be passed this year. The company is holding an educational seminar on UDI readiness on Monday, September 9 in Morristown, New Jersey. UDI will require medical device makers to place a unique numeric or alphanumeric code on every device or label, which will include such information as batch number, serial number, and/or expiration date. The Food and Drug Administration (FDA) anticipates that the regulation will enable improved patient safety and quicker identification of product problems.

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