Transo-Pharm GmbH works globally to supply Active Pharmaceutical Ingredients adhering to the highest quality & GMP standards.
01 1Transo-Pharm Handels GmbH
02 13M Company
03 1Amphastar Pharmaceuticals
04 1Cambrex Corporation
05 1Derivados Quimicos SAU
06 2GLAND PHARMA LIMITED
07 1Olon S.p.A
08 1Phlow Corporation
09 1Sun Pharmaceutical Industries Limited
10 1Viatris
11 1Wockhardt
Transo-Pharm GmbH works globally to supply Active Pharmaceutical Ingredients adhering to the highest quality & GMP standards.
GDUFA
DMF Review : Complete
Rev. Date : 2018-01-11
Pay. Date : 2016-12-28
DMF Number : 30997
Submission : 2016-09-20
Status :
Type : II
100
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A nchembio747-comp9 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of nchembio747-comp9, including repackagers and relabelers. The FDA regulates nchembio747-comp9 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. nchembio747-comp9 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A nchembio747-comp9 DMF (Drug Master File) is a document detailing the whole manufacturing process of nchembio747-comp9 active pharmaceutical ingredient (API) in detail. Different forms of nchembio747-comp9 DMFs exist exist since differing nations have different regulations, such as nchembio747-comp9 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
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