01 AMINO GMBH Frellstedt DE (1)
02 Ajinomoto Co., Inc. Tokyo JP (3)
03 KYOWA HAKKO BIO CO., LTD. Tokyo JP (2)
04 SHANGHAI KYOWA AMINO ACID CO., LTD. Shanghai CN (2)
01 Histidine (4)
02 Histidine Hydrochloride Monohydrate (3)
03 Histidine, SA (1)
01 Germany (1)
02 Japan (7)
01 Valid (8)
80
PharmaCompass offers a list of L-Histidine API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right L-Histidine manufacturer or L-Histidine supplier for your needs.
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PharmaCompass also assists you with knowing the L-Histidine API Price utilized in the formulation of products. L-Histidine API Price is not always fixed or binding as the L-Histidine Price is obtained through a variety of data sources. The L-Histidine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A MolPort-001-792-384 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of MolPort-001-792-384, including repackagers and relabelers. The FDA regulates MolPort-001-792-384 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. MolPort-001-792-384 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 MolPort-001-792-384 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A MolPort-001-792-384 supplier is an individual or a company that provides MolPort-001-792-384 active pharmaceutical ingredient (API) or MolPort-001-792-384 finished formulations upon request. The MolPort-001-792-384 suppliers may include MolPort-001-792-384 API manufacturers, exporters, distributors and traders.
click here to find a list of MolPort-001-792-384 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A MolPort-001-792-384 CEP of the European Pharmacopoeia monograph is often referred to as a MolPort-001-792-384 Certificate of Suitability (COS). The purpose of a MolPort-001-792-384 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of MolPort-001-792-384 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of MolPort-001-792-384 to their clients by showing that a MolPort-001-792-384 CEP has been issued for it. The manufacturer submits a MolPort-001-792-384 CEP (COS) as part of the market authorization procedure, and it takes on the role of a MolPort-001-792-384 CEP holder for the record. Additionally, the data presented in the MolPort-001-792-384 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the MolPort-001-792-384 DMF.
A MolPort-001-792-384 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. MolPort-001-792-384 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 MolPort-001-792-384 suppliers with CEP (COS) on PharmaCompass.
We have 4 companies offering MolPort-001-792-384
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