| Health / Medical Topics |
Type of Form
A description of a form which accompanies regulatory submissions. (Food and Drug Administration)
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Terminology used in Individual Case Safety Reports to specify a type of follow-up after an initial report has been submitted, section H2…
Terminology used in Individual Case Safety Reports for identifying the type of event (adverse event or product problem), section B1 of FDA…
A particular category of events regarded as having particular characteristics, qualities, and/or defined similarities.
A category of results of drug adverse reaction or drug interaction.
Generic category of medical device within the device classification established by FDA. It is used as part of regulatory product submission…
Identification and clinical investigation of disease contacts.
