viernes, 4 de abril de 2014

CDRH Industry: Types of Communication During the Review of Medical Device Submissions - Guidance for Industry and FDA Staff

A guidance for Industry and Food and Drug Administration staff about the types of communication during the review of medical device submissions has recently been posted.  For more information, please see http://www.fda.gov/MedicalDevices/DeviceRegulationandGuidance/GuidanceDocuments/ucm341918.htm

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