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