Evonik's CDMO solutions for APIs and HPAPIs: It specializes where the client needs it most!
01 2Evonik Rexim S. A. S.
02 1Ajinomoto Co., Inc.
03 1Sekisui Medical Co., Ltd.
04 2Taenaka Mining Co., Ltd.
Evonik's CDMO solutions for APIs and HPAPIs: It specializes where the client needs it most!
Registration Number : 226MF10122
Registrant's Address : 33, Rue de Verdun Ham, France
Initial Date of Registration : 2014-06-18
Latest Date of Registration : 2019-07-26
Evonik's CDMO solutions for APIs and HPAPIs: It specializes where the client needs it most!
Registration Number : 225MF10190
Registrant's Address : 33, Rue de Verdun Ham, France
Initial Date of Registration : 2013-10-09
Latest Date of Registration : 2013-10-09
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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 (S)-2-Aminopentanedioate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of (S)-2-Aminopentanedioate, including repackagers and relabelers. The FDA regulates (S)-2-Aminopentanedioate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. (S)-2-Aminopentanedioate 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 (S)-2-Aminopentanedioate supplier is an individual or a company that provides (S)-2-Aminopentanedioate active pharmaceutical ingredient (API) or (S)-2-Aminopentanedioate finished formulations upon request. The (S)-2-Aminopentanedioate suppliers may include (S)-2-Aminopentanedioate API manufacturers, exporters, distributors and traders.
click here to find a list of (S)-2-Aminopentanedioate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The (S)-2-Aminopentanedioate Drug Master File in Japan ((S)-2-Aminopentanedioate JDMF) empowers (S)-2-Aminopentanedioate API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the (S)-2-Aminopentanedioate JDMF during the approval evaluation for pharmaceutical products. At the time of (S)-2-Aminopentanedioate JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of (S)-2-Aminopentanedioate suppliers with JDMF on PharmaCompass.
We have 4 companies offering (S)-2-Aminopentanedioate
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