01 1Rhodia Organique SAS
01 1PARATRIFLUOROMETHOXYANILINE
01 1France
01 1Inactive
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 15831
Submission : 2002-01-30
Status : Inactive
Type : II
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A Trifluoromethoxyaniline manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Trifluoromethoxyaniline, including repackagers and relabelers. The FDA regulates Trifluoromethoxyaniline manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Trifluoromethoxyaniline API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Trifluoromethoxyaniline supplier is an individual or a company that provides Trifluoromethoxyaniline active pharmaceutical ingredient (API) or Trifluoromethoxyaniline finished formulations upon request. The Trifluoromethoxyaniline suppliers may include Trifluoromethoxyaniline API manufacturers, exporters, distributors and traders.
click here to find a list of Trifluoromethoxyaniline suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A Trifluoromethoxyaniline DMF (Drug Master File) is a document detailing the whole manufacturing process of Trifluoromethoxyaniline active pharmaceutical ingredient (API) in detail. Different forms of Trifluoromethoxyaniline DMFs exist exist since differing nations have different regulations, such as Trifluoromethoxyaniline USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Trifluoromethoxyaniline DMF submitted to regulatory agencies in the US is known as a USDMF. Trifluoromethoxyaniline USDMF includes data on Trifluoromethoxyaniline's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Trifluoromethoxyaniline USDMF is kept confidential to protect the manufacturer’s intellectual property.
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