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.
01 2Japanese Pharmacopoeia L- glutamic acid (production only)
02 1L- glutamic acid L- arginine
03 2L- glutamic acid L-Glutamic acid
04 1Outsiders regulations L- glutamic acid (production only)
01 2Germany
02 4Japan
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
Japanese Pharmacopoeia L-Glutamic Acid (for manufacturing only)
Registration Number : 224MF10004
Registrant's Address : 1-15-1 Kyobashi, Chuo-ku, Tokyo
Initial Date of Registration : 2012-01-18
Latest Date of Registration : 2012-01-18
Registration Number : 217MF10762
Registrant's Address : 2-1-3 Nihonbashi, Chuo-ku, Tokyo
Initial Date of Registration : 2005-10-20
Latest Date of Registration : 2010-01-07
Extra-official regulations L-glutamic acid (for manufacturing only)
Registration Number : 217MF10282
Registrant's Address : 452 Oshiba, Mobara City, Chiba Prefecture
Initial Date of Registration : 2005-06-20
Latest Date of Registration : 2007-07-02
Japanese Pharmacopoeia L-Glutamic Acid (for manufacturing purposes only)
Registration Number : 224MF10003
Registrant's Address : 452 Oshiba, Mobara City, Chiba Prefecture
Initial Date of Registration : 2012-01-18
Latest Date of Registration : 2012-01-18
A Glutamic Acid manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Glutamic Acid, including repackagers and relabelers. The FDA regulates Glutamic Acid manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Glutamic Acid 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 Glutamic Acid manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Glutamic Acid supplier is an individual or a company that provides Glutamic Acid active pharmaceutical ingredient (API) or Glutamic Acid finished formulations upon request. The Glutamic Acid suppliers may include Glutamic Acid API manufacturers, exporters, distributors and traders.
click here to find a list of Glutamic Acid 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 Glutamic Acid Drug Master File in Japan (Glutamic Acid JDMF) empowers Glutamic Acid 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 Glutamic Acid JDMF during the approval evaluation for pharmaceutical products. At the time of Glutamic Acid 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 Glutamic Acid suppliers with JDMF on PharmaCompass.
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