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