A Freon 12, R-12, CFC-12, P-12, Propellant 12, Halon 122, Arcton 6, Arcton 12, E940 DMF (Drug Master File) is a document detailing the whole manufacturing process of Freon 12, R-12, CFC-12, P-12, Propellant 12, Halon 122, Arcton 6, Arcton 12, E940 active pharmaceutical ingredient (API) in detail. Different forms of Freon 12, R-12, CFC-12, P-12, Propellant 12, Halon 122, Arcton 6, Arcton 12, E940 DMFs exist exist since differing nations have different regulations, such as Freon 12, R-12, CFC-12, P-12, Propellant 12, Halon 122, Arcton 6, Arcton 12, E940 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
										A Freon 12, R-12, CFC-12, P-12, Propellant 12, Halon 122, Arcton 6, Arcton 12, E940 DMF submitted to regulatory agencies in the US is known as a USDMF. Freon 12, R-12, CFC-12, P-12, Propellant 12, Halon 122, Arcton 6, Arcton 12, E940 USDMF includes data on Freon 12, R-12, CFC-12, P-12, Propellant 12, Halon 122, Arcton 6, Arcton 12, E940's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Freon 12, R-12, CFC-12, P-12, Propellant 12, Halon 122, Arcton 6, Arcton 12, E940 USDMF is kept confidential to protect the manufacturer’s intellectual property.
										click here to find a list of Freon 12, R-12, CFC-12, P-12, Propellant 12, Halon 122, Arcton 6, Arcton 12, E940 suppliers with USDMF on PharmaCompass.