Submitting Documentation for the Manufacture of and Controls for Drug Products
Title:
Submitting Documentation for the Manufacture of and Controls for Drug Products
Origin/Publisher:
Freedom of Information Staff, (HFI 35), Food and Drug Administration, Rm. 12 A - 30, 5600 Fishers Lane, Rockville, MD 20857, USA, http://www.fda.gov/cder/guidance
Document Type:
FDA Guidance for Industry
Content:
Submitting Documentation for the Manufacture of and Controls for Drug Products