| GMP Facility | A production facility or clinical trial materials pilot plant for the manufacture of pharmaceutical products. It includes the manufacturing space, the storage warehouse for raw and finished product, and support lab areas. A GMP facility operates under the guidelines established by the CFR (Code of Federal Regulations) Title 21, Parts 225 (Current Good Manufacturing for Medicated Feeds - Subpart B), and Part 226 (Current Good Manufacturing Practice for Type A Medicated Articles - Subpart B). |
