01 1S D Fine Chem Limited
01 1CHLOROFORM BP
01 1India
01 1Active
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 28849
Submission : 2014-11-20
Status : Active
Type : IV
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A Cloroformio manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cloroformio, including repackagers and relabelers. The FDA regulates Cloroformio manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cloroformio API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Cloroformio manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Cloroformio supplier is an individual or a company that provides Cloroformio active pharmaceutical ingredient (API) or Cloroformio finished formulations upon request. The Cloroformio suppliers may include Cloroformio API manufacturers, exporters, distributors and traders.
click here to find a list of Cloroformio suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A Cloroformio DMF (Drug Master File) is a document detailing the whole manufacturing process of Cloroformio active pharmaceutical ingredient (API) in detail. Different forms of Cloroformio DMFs exist exist since differing nations have different regulations, such as Cloroformio USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Cloroformio DMF submitted to regulatory agencies in the US is known as a USDMF. Cloroformio USDMF includes data on Cloroformio's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Cloroformio USDMF is kept confidential to protect the manufacturer’s intellectual property.
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