FDA Guidance for Industry: Type V DMFs for CDER-Led Combination Products Using Device Constituent Parts With Electronics or Software

FDA Guidance for Industry: Type V DMFs for CDER-Led Combination Products Using Device Constituent Parts With Electronics or Software

A drug master file (DMF) is a voluntary submission to 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