01 2Myonaka Mining Co., Ltd.
02 1Nippon Protein Co., Ltd.
03 1Nippon Rikagaku Yakuhin Co., Ltd.
01 1Japanese Pharmacopoeia L- cysteine
02 1Japanese Pharmacopoeia L- cystine (production only)
03 2Outsiders regulations L- cystine (production only)
01 4Japan
Japanese Pharmacopoeia L-Cysteine
Registration Number : 219MF10338
Registrant's Address : 4-2-2 Nihonbashi Honcho, Chuo-ku, Tokyo
Initial Date of Registration : 2007-11-21
Latest Date of Registration : 2007-11-21
Non-pharmaceutical standard L-cystine (for manufacturing only)
Registration Number : 218MF11012
Registrant's Address : 575-1 Shimada-cho, Ashikaga City, Tochigi Prefecture
Initial Date of Registration : 2006-12-18
Latest Date of Registration : 2006-12-18
Japanese Pharmacopoeia L-Cystine (for manufacturing purposes only)
Registration Number : 225MF10115
Registrant's Address : 452 Ooshiba, Mobara City, Chiba Prefecture
Initial Date of Registration : 2013-06-07
Latest Date of Registration : 2013-06-07
Non-pharmaceutical standard L-cystine (for manufacturing only)
Registration Number : 217MF10284
Registrant's Address : 452 Ooshiba, Mobara City, Chiba Prefecture
Initial Date of Registration : 2005-06-20
Latest Date of Registration : 2007-07-26
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PharmaCompass offers a list of Cystine API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Cystine manufacturer or Cystine supplier for your needs.
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A L-Cystine, Vetec(TM) reagent grade, 98% manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of L-Cystine, Vetec(TM) reagent grade, 98%, including repackagers and relabelers. The FDA regulates L-Cystine, Vetec(TM) reagent grade, 98% manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. L-Cystine, Vetec(TM) reagent grade, 98% 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 L-Cystine, Vetec(TM) reagent grade, 98% manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A L-Cystine, Vetec(TM) reagent grade, 98% supplier is an individual or a company that provides L-Cystine, Vetec(TM) reagent grade, 98% active pharmaceutical ingredient (API) or L-Cystine, Vetec(TM) reagent grade, 98% finished formulations upon request. The L-Cystine, Vetec(TM) reagent grade, 98% suppliers may include L-Cystine, Vetec(TM) reagent grade, 98% API manufacturers, exporters, distributors and traders.
click here to find a list of L-Cystine, Vetec(TM) reagent grade, 98% suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA 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 L-Cystine, Vetec(TM) reagent grade, 98% Drug Master File in Japan (L-Cystine, Vetec(TM) reagent grade, 98% JDMF) empowers L-Cystine, Vetec(TM) reagent grade, 98% 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 L-Cystine, Vetec(TM) reagent grade, 98% JDMF during the approval evaluation for pharmaceutical products. At the time of L-Cystine, Vetec(TM) reagent grade, 98% 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 L-Cystine, Vetec(TM) reagent grade, 98% suppliers with JDMF on PharmaCompass.
We have 3 companies offering L-Cystine, Vetec(TM) reagent grade, 98%
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