01 1Ajinomoto Co., Inc. Tokyo JP
01 1Isoleucine, Limeira Amino Acid site
01 1Japan
01 1Valid
Isoleucine, Limeira Amino Acid Site
Certificate Number : R1-CEP 2009-100 - Rev 00
Status : Valid
Issue Date : 2014-12-16
Type : Chemical
Substance Number : 770
83
PharmaCompass offers a list of Amino Acids Mixture 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 Amino Acids Mixture manufacturer or Amino Acids Mixture supplier for your needs.
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PharmaCompass also assists you with knowing the Amino Acids Mixture API Price utilized in the formulation of products. Amino Acids Mixture API Price is not always fixed or binding as the Amino Acids Mixture Price is obtained through a variety of data sources. The Amino Acids Mixture Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A HEPATAMINE 8% manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of HEPATAMINE 8%, including repackagers and relabelers. The FDA regulates HEPATAMINE 8% manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. HEPATAMINE 8% 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 HEPATAMINE 8% supplier is an individual or a company that provides HEPATAMINE 8% active pharmaceutical ingredient (API) or HEPATAMINE 8% finished formulations upon request. The HEPATAMINE 8% suppliers may include HEPATAMINE 8% API manufacturers, exporters, distributors and traders.
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A HEPATAMINE 8% CEP of the European Pharmacopoeia monograph is often referred to as a HEPATAMINE 8% Certificate of Suitability (COS). The purpose of a HEPATAMINE 8% CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of HEPATAMINE 8% EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of HEPATAMINE 8% to their clients by showing that a HEPATAMINE 8% CEP has been issued for it. The manufacturer submits a HEPATAMINE 8% CEP (COS) as part of the market authorization procedure, and it takes on the role of a HEPATAMINE 8% CEP holder for the record. Additionally, the data presented in the HEPATAMINE 8% CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the HEPATAMINE 8% DMF.
A HEPATAMINE 8% CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. HEPATAMINE 8% CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
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