01 1Ajinomoto Co., Inc. Tokyo JP
01 1Arginine, SA
01 1Japan
01 1Valid
Certificate Number : R0-CEP 2022-190 - Rev 00
Status : Valid
Issue Date : 2022-09-29
Type : Chemical
Substance Number : 806
11
PharmaCompass offers a list of L-Arginine 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-Arginine manufacturer or L-Arginine supplier for your needs.
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PharmaCompass also assists you with knowing the L-Arginine API Price utilized in the formulation of products. L-Arginine API Price is not always fixed or binding as the L-Arginine Price is obtained through a variety of data sources. The L-Arginine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A arg manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of arg, including repackagers and relabelers. The FDA regulates arg manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. arg 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 arg manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A arg supplier is an individual or a company that provides arg active pharmaceutical ingredient (API) or arg finished formulations upon request. The arg suppliers may include arg API manufacturers, exporters, distributors and traders.
click here to find a list of arg suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A arg CEP of the European Pharmacopoeia monograph is often referred to as a arg Certificate of Suitability (COS). The purpose of a arg CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of arg EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of arg to their clients by showing that a arg CEP has been issued for it. The manufacturer submits a arg CEP (COS) as part of the market authorization procedure, and it takes on the role of a arg CEP holder for the record. Additionally, the data presented in the arg CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the arg DMF.
A arg CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. arg 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 arg suppliers with CEP (COS) on PharmaCompass.
