Evonik Health Care is the innovation hub for leading life science companies
01 1EVONIK REXIM S.A.S. Ham FR
02 1AMINO GMBH Frellstedt DE
03 1Ajinomoto Co., Inc. Tokyo JP
04 1Taenaka Kogyo Co., Ltd. Mobara-shi JP
01 4Glutamic Acid
01 1Gabon
02 1Germany
03 2Japan
01 4Valid
Evonik Health Care is the innovation hub for leading life science companies
Evonik Health Care is the innovation hub for leading life science companies
Certificate Number : CEP 2009-311 - Rev 01
Status : Valid
Issue Date : 2024-01-29
Type : Chemical
Substance Number : 750
Certificate Number : R1-CEP 1998-066 - Rev 01
Status : Valid
Issue Date : 2006-09-29
Type : Chemical
Substance Number : 750
Certificate Number : R0-CEP 2019-279 - Rev 00
Status : Valid
Issue Date : 2021-05-18
Type : Chemical
Substance Number : 750
Certificate Number : R1-CEP 2000-205 - Rev 02
Status : Valid
Issue Date : 2012-08-13
Type : Chemical
Substance Number : 750
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PharmaCompass offers a list of L-Glutamic Acid 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-Glutamic Acid manufacturer or L-Glutamic Acid supplier for your needs.
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PharmaCompass also assists you with knowing the L-Glutamic Acid API Price utilized in the formulation of products. L-Glutamic Acid API Price is not always fixed or binding as the L-Glutamic Acid Price is obtained through a variety of data sources. The L-Glutamic Acid Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A HMDB00148 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of HMDB00148, including repackagers and relabelers. The FDA regulates HMDB00148 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. HMDB00148 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 HMDB00148 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A HMDB00148 supplier is an individual or a company that provides HMDB00148 active pharmaceutical ingredient (API) or HMDB00148 finished formulations upon request. The HMDB00148 suppliers may include HMDB00148 API manufacturers, exporters, distributors and traders.
click here to find a list of HMDB00148 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A HMDB00148 CEP of the European Pharmacopoeia monograph is often referred to as a HMDB00148 Certificate of Suitability (COS). The purpose of a HMDB00148 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of HMDB00148 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of HMDB00148 to their clients by showing that a HMDB00148 CEP has been issued for it. The manufacturer submits a HMDB00148 CEP (COS) as part of the market authorization procedure, and it takes on the role of a HMDB00148 CEP holder for the record. Additionally, the data presented in the HMDB00148 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the HMDB00148 DMF.
A HMDB00148 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. HMDB00148 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 HMDB00148 suppliers with CEP (COS) on PharmaCompass.
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