Evonik's CDMO solutions for APIs and HPAPIs: It specializes where the client needs it most!
01 1Evonik Rexim (Nanning) Pharmaceutical Co. , Ltd.
02 1Evonik Rexim S. A. S.
03 1Ajinomoto Health & Nutrition North America, Inc.
04 1Kamiishiwabasa Acid Co., Ltd.
05 1Kyowa Hakko Bio Co., Ltd.
06 1Shanghai Ajinomoto Amino Acid Co., Ltd.
Evonik's CDMO solutions for APIs and HPAPIs: It specializes where the client needs it most!
Registration Number : 218MF10975
Registrant's Address : No. 46 Wenjiang Road, Wuming District, Nanning, 530199, Guangxi, P. R. China
Initial Date of Registration : 2006-12-01
Latest Date of Registration : 2019-06-18
Evonik's CDMO solutions for APIs and HPAPIs: It specializes where the client needs it most!
Registration Number : 218MF10656
Registrant's Address : 33, Rue De Verdun Ham France
Initial Date of Registration : 2006-07-24
Latest Date of Registration : 2006-07-24
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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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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 05129_FLUKA Drug Master File in Japan (05129_FLUKA JDMF) empowers 05129_FLUKA 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 05129_FLUKA JDMF during the approval evaluation for pharmaceutical products. At the time of 05129_FLUKA JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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