Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B907cb6af91b1689da7c45fa39c4f4b51> ?p ?o ?g. }
Showing items 1 to 5 of
5
with 100 items per page.
- B907cb6af91b1689da7c45fa39c4f4b51 NCIT_P378 "PQCMC" @default.
- B907cb6af91b1689da7c45fa39c4f4b51 type Axiom @default.
- B907cb6af91b1689da7c45fa39c4f4b51 annotatedProperty NCIT_P325 @default.
- B907cb6af91b1689da7c45fa39c4f4b51 annotatedSource NCIT_C70877 @default.
- B907cb6af91b1689da7c45fa39c4f4b51 annotatedTarget "Drug master files (DMFs) are submissions to FDA used to provide confidential, detailed information about facilities, processes, or articles used in the manufacturing, processing, packaging, and storing of human drug products. They 1) Allow parties to reference material without disclosing DMF contents to those parties. 2) Are not required by statute or regulation. 3) Are neither approved nor disapproved. Instead, FDA reviews the technical contents of DMFs in connection with the review of applications that reference them (e.g., NDAs, ANDAs, INDs, BLAs)." @default.