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Research / Unique Device Identification / Medical device / Center for Devices and Radiological Health / Adverse Event Reporting System / Clinical research / Electronic health record / Adverse event / Premarket approval / Food and Drug Administration / Medicine / Health


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Company

Sentinel / rOle Of Sentinel / /

Country

United States / /

Facility

Institute of Medicine / /

IndustryTerm

medical device / cardiovascular devices / effec tive products / supply chain / public law / regulat ed medical products / event reporting systems / distributed data systems / manufacturing lot / pediatric intensive care unit devices / technology adoption / postmarket safety sur veillance systems / surveillance network / thorough premarket product / integrated health systems / clinical information systems / medi cal devices / near real-time / med ical device / non-clinical device / regulated medical products / marketed devices / informa tion technology / fOOd / /

MedicalCondition

device-associated serious injuries / serious injuries / /

Organization

FDA's Center for Devices / Food and Drug Administration / FDA’s MDR / Institute of Medicine / Radiological Health / FDA's Center for Devices and Radiological Health / Fda / Medicare / /

Position

Secretary of Health / Commissioner / /

Product

Strengthening / medical device POStmarket Surveillance SyStem FDA / POStmarket Surveillance SyStem FDA / /

Technology

informa tion technology / /

URL

http /

SocialTag