A Poly[oxy(methyl-1,2-ethanediyl)], .alpha.-hydro-.omega.-hydroxy- DMF (Drug Master File) is a document detailing the whole manufacturing process of Poly[oxy(methyl-1,2-ethanediyl)], .alpha.-hydro-.omega.-hydroxy- active pharmaceutical ingredient (API) in detail. Different forms of Poly[oxy(methyl-1,2-ethanediyl)], .alpha.-hydro-.omega.-hydroxy- DMFs exist exist since differing nations have different regulations, such as Poly[oxy(methyl-1,2-ethanediyl)], .alpha.-hydro-.omega.-hydroxy- USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Poly[oxy(methyl-1,2-ethanediyl)], .alpha.-hydro-.omega.-hydroxy- DMF submitted to regulatory agencies in the US is known as a USDMF. Poly[oxy(methyl-1,2-ethanediyl)], .alpha.-hydro-.omega.-hydroxy- USDMF includes data on Poly[oxy(methyl-1,2-ethanediyl)], .alpha.-hydro-.omega.-hydroxy-'s chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Poly[oxy(methyl-1,2-ethanediyl)], .alpha.-hydro-.omega.-hydroxy- USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Poly[oxy(methyl-1,2-ethanediyl)], .alpha.-hydro-.omega.-hydroxy- suppliers with USDMF on PharmaCompass.