01 1Ajinomoto Co., Inc. Tokyo JP
01 1Histidine Hydrochloride Monohydrate, SA
01 1Japan
01 1Valid
Histidine Hydrochloride Monohydrate, SA
Certificate Number : CEP 2023-213 - Rev 00
Status : Valid
Issue Date : 2024-03-04
Type : Chemical
Substance Number : 910
A Histidine Dihydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Histidine Dihydrochloride, including repackagers and relabelers. The FDA regulates Histidine Dihydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Histidine Dihydrochloride 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 Histidine Dihydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Histidine Dihydrochloride supplier is an individual or a company that provides Histidine Dihydrochloride active pharmaceutical ingredient (API) or Histidine Dihydrochloride finished formulations upon request. The Histidine Dihydrochloride suppliers may include Histidine Dihydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Histidine Dihydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Histidine Dihydrochloride CEP of the European Pharmacopoeia monograph is often referred to as a Histidine Dihydrochloride Certificate of Suitability (COS). The purpose of a Histidine Dihydrochloride CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Histidine Dihydrochloride EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Histidine Dihydrochloride to their clients by showing that a Histidine Dihydrochloride CEP has been issued for it. The manufacturer submits a Histidine Dihydrochloride CEP (COS) as part of the market authorization procedure, and it takes on the role of a Histidine Dihydrochloride CEP holder for the record. Additionally, the data presented in the Histidine Dihydrochloride CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Histidine Dihydrochloride DMF.
A Histidine Dihydrochloride CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Histidine Dihydrochloride CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
click here to find a list of Histidine Dihydrochloride suppliers with CEP (COS) on PharmaCompass.
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