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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