GMP: FDA publishes Proposals on Harmonised Identification of Medical Devices (UDI)
06.09.2012
The FDA announced via its Center for Devices and Radiological Health (CDRH) - which is also responsible for medical devices - the publication of requirements on harmonised designation of medical devices (Unique Device Identification System, UDI system).
Źródło wiadomośći: http://www.gmp-compliance.org/eca_news_3285_7298,7381,7451.html
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