01 1Atul Bioscience Ltd
01 1CLIOQUINOL
01 1India
01 1Inactive
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 9078
Submission : 1991-04-20
Status : Inactive
Type : II
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A Vioform manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Vioform, including repackagers and relabelers. The FDA regulates Vioform manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Vioform 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 Vioform manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Vioform supplier is an individual or a company that provides Vioform active pharmaceutical ingredient (API) or Vioform finished formulations upon request. The Vioform suppliers may include Vioform API manufacturers, exporters, distributors and traders.
click here to find a list of Vioform suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A Vioform DMF (Drug Master File) is a document detailing the whole manufacturing process of Vioform active pharmaceutical ingredient (API) in detail. Different forms of Vioform DMFs exist exist since differing nations have different regulations, such as Vioform USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Vioform DMF submitted to regulatory agencies in the US is known as a USDMF. Vioform USDMF includes data on Vioform's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Vioform USDMF is kept confidential to protect the manufacturer’s intellectual property.
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