THE UDI Final Rule Interactive Compliance Calendar




The FDA Final Rule on unique device identification (UDI) for medical devices is out. Covering both labelling and the GUDID database, manufacturers need to assess their current technical capabilities - both hardware and software - and work out how much they need to do in order to comply. Ahead of the Medical Device UDIs & Traceability Forum, taking place 20 - 22 May, 2014 in Munich, Germany, Pharma IQ has put together this one-page compliance calendar to help you understand what impact the September 2013 FDA Final Rule on unique device identification will have on your business. 
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