Health / Medical Topics |
FDA Center For Devices and Radiological Health Terminology
Terminology used in individual case reports for voluntary and mandatory reporting of adverse reactions or adverse events during both pre and post approval periods of medical device development and usage. (NCI Thesaurus)
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A set of terminology created to support the efforts of the FDA CDRH Global Unique Device Identification Database project.
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Terminology codelist used to describe the principal observations for human clinical and non-human non-clinical studies for the FDA CDA guide.
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This gene may be involved in B cell receptor signaling.