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Medical Case Reports Software In Usa Pennsylvania
2 software items found
by:RegScan - by Enhesa based inWilliamsport, PENNSYLVANIA (USA)
The medical device reporting (MDR) requirements of 21 CFR 803 apply to manufacturers, importers, distributers, and device user facilities in the United States. Such facilities are required to report adverse device-related events to the Food and Drug Administration (FDA) or the device manufacturer, and occasionally to both. These requirements are supplemental to the quality system requirements of ...
Manufactured by:Syncro Medical based inLanghorne, PENNSYLVANIA (USA)
Cutting edge medical instrument manufacturers are uncovering the hidden value of the data collected and generated by their systems. With Syncro Medical’s help, they’re using this data to gain new insights, both Clinical and Operational. Clinical healthcare analytics focus primarily on the patient, for example patient outcomes or medication/ device compliance. Operational medical ...