01 1Chengzhi Life Science Co Ltd
01 1D-RIBOSE
01 1China
01 1Active
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 28950
Submission : 2014-12-08
Status : Active
Type : II
A Ribose manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ribose, including repackagers and relabelers. The FDA regulates Ribose manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ribose 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 Ribose manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Ribose supplier is an individual or a company that provides Ribose active pharmaceutical ingredient (API) or Ribose finished formulations upon request. The Ribose suppliers may include Ribose API manufacturers, exporters, distributors and traders.
click here to find a list of Ribose suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Ribose DMF (Drug Master File) is a document detailing the whole manufacturing process of Ribose active pharmaceutical ingredient (API) in detail. Different forms of Ribose DMFs exist exist since differing nations have different regulations, such as Ribose USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Ribose DMF submitted to regulatory agencies in the US is known as a USDMF. Ribose USDMF includes data on Ribose's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Ribose USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Ribose suppliers with USDMF on PharmaCompass.
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