Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B07f65d0b5c53fc96d8d5c99012e26d71> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- B07f65d0b5c53fc96d8d5c99012e26d71 NCIT_P378 "FDA" @default.
- B07f65d0b5c53fc96d8d5c99012e26d71 NCIT_P381 "eCTD" @default.
- B07f65d0b5c53fc96d8d5c99012e26d71 type Axiom @default.
- B07f65d0b5c53fc96d8d5c99012e26d71 annotatedProperty NCIT_P325 @default.
- B07f65d0b5c53fc96d8d5c99012e26d71 annotatedSource NCIT_C70877 @default.
- B07f65d0b5c53fc96d8d5c99012e26d71 annotatedTarget "A Drug Master File (DMF) is a submission to the Food and Drug Administration (FDA) that may be used to provide confidential detailed information about facilities, processes, or articles used in the manufacturing, processing, packaging, and storing of one or more human drugs. The submission of a DMF is not required by law or FDA regulation. A DMF is submitted solely at the discretion of the holder. The information contained in the DMF may be used to support an Investigational New Drug Application (IND), a New Drug Application (NDA), an Abbreviated New Drug Application (ANDA), another DMF, an Export Application, or amendments and supplements to any of these." @default.