Evonik's CDMO solutions for APIs and HPAPIs: It specializes where the client needs it most!
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's CDMO solutions for APIs and HPAPIs: It specializes where the client needs it most!
Evonik's CDMO solutions for APIs and HPAPIs: It specializes where the client needs it most!
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.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred L-Glutamic Acid manufacturer or L-Glutamic Acid supplier.
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 49449_FLUKA manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 49449_FLUKA, including repackagers and relabelers. The FDA regulates 49449_FLUKA manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 49449_FLUKA 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 49449_FLUKA manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A 49449_FLUKA supplier is an individual or a company that provides 49449_FLUKA active pharmaceutical ingredient (API) or 49449_FLUKA finished formulations upon request. The 49449_FLUKA suppliers may include 49449_FLUKA API manufacturers, exporters, distributors and traders.
click here to find a list of 49449_FLUKA suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A 49449_FLUKA CEP of the European Pharmacopoeia monograph is often referred to as a 49449_FLUKA Certificate of Suitability (COS). The purpose of a 49449_FLUKA CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of 49449_FLUKA EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of 49449_FLUKA to their clients by showing that a 49449_FLUKA CEP has been issued for it. The manufacturer submits a 49449_FLUKA CEP (COS) as part of the market authorization procedure, and it takes on the role of a 49449_FLUKA CEP holder for the record. Additionally, the data presented in the 49449_FLUKA CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the 49449_FLUKA DMF.
A 49449_FLUKA CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. 49449_FLUKA 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 49449_FLUKA suppliers with CEP (COS) on PharmaCompass.
We have 4 companies offering 49449_FLUKA
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