Evonik's CDMO solutions for APIs and HPAPIs: It specializes where the client needs it most!
01 1EVONIK REXIM (NANNING) PHARMACEUTICAL CO., LTD. Nanning CN
02 1AMINO GMBH Frellstedt DE
03 3Ajinomoto Co., Inc. Tokyo JP
04 1KYOWA HAKKO BIO CO., LTD. Tokyo JP
05 1Rexim SAS Ham FR
06 1SHANGHAI KYOWA AMINO ACID CO., LTD. Shanghai CN
01 6Alanine
02 1Alanine, II
03 1Alanine, SA
01 1France
02 1Gabon
03 1Germany
04 5Japan
01 7Valid
02 1Withdrawn by Holder
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 : R1-CEP 2004-086 - Rev 07
Status : Valid
Issue Date : 2023-08-24
Type : Chemical
Substance Number : 752
Certificate Number : R1-CEP 1998-105 - Rev 05
Status : Valid
Issue Date : 2018-06-22
Type : Chemical
Substance Number : 752
Certificate Number : R1-CEP 2014-002 - Rev 00
Status : Valid
Issue Date : 2020-10-20
Type : Chemical
Substance Number : 752
Certificate Number : CEP 2018-145 - Rev 01
Status : Valid
Issue Date : 2023-12-20
Type : Chemical
Substance Number : 752
Certificate Number : CEP 2013-157 - Rev 02
Status : Valid
Issue Date : 2025-01-20
Type : Chemical
Substance Number : 752
Certificate Number : R1-CEP 1999-013 - Rev 02
Status : Valid
Issue Date : 2014-07-30
Type : Chemical
Substance Number : 752
Certificate Number : R1-CEP 1997-053 - Rev 02
Status : Withdrawn by Holder
Issue Date : 2007-02-27
Type : Chemical
Substance Number : 752
Certificate Number : R1-CEP 2007-351 - Rev 01
Status : Valid
Issue Date : 2023-01-12
Type : Chemical
Substance Number : 752
77
PharmaCompass offers a list of L-Alanine API 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-Alanine API manufacturer or L-Alanine API supplier for your needs.
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A 05129_FLUKA manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 05129_FLUKA, including repackagers and relabelers. The FDA regulates 05129_FLUKA manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 05129_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.
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A 05129_FLUKA supplier is an individual or a company that provides 05129_FLUKA active pharmaceutical ingredient (API) or 05129_FLUKA finished formulations upon request. The 05129_FLUKA suppliers may include 05129_FLUKA API manufacturers, exporters, distributors and traders.
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A 05129_FLUKA CEP of the European Pharmacopoeia monograph is often referred to as a 05129_FLUKA Certificate of Suitability (COS). The purpose of a 05129_FLUKA CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of 05129_FLUKA EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of 05129_FLUKA to their clients by showing that a 05129_FLUKA CEP has been issued for it. The manufacturer submits a 05129_FLUKA CEP (COS) as part of the market authorization procedure, and it takes on the role of a 05129_FLUKA CEP holder for the record. Additionally, the data presented in the 05129_FLUKA CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the 05129_FLUKA DMF.
A 05129_FLUKA CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. 05129_FLUKA 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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