News | News By Subject | News by Disease News By Date | Search News
Get Our FREE
Industry eNewsletter
email:    
   

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



8/22/2013 9:44:09 AM

Get the latest biotech news where you want it. Sign up for the free GenePool newsletter today!

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.

Help employers find you! Check out all the jobs and post your resume.

Read at BioSpace.com


comments powered by Disqus
   

ADD TO DEL.ICIO.US    ADD TO DIGG    ADD TO FURL    ADD TO STUMBLEUPON    ADD TO TECHNORATI FAVORITES