01 1Sanwa Chemical Co., Ltd.
01 1Japan Pharmaceutical Codex mesylate address Roh chromium mono amino guanidine (production only)
01 1Japan
Registration Number : 218MF10557
Registrant's Address : 24-8, Tamura 9-chome, Hiratsuka City, Kanagawa Prefecture
Initial Date of Registration : 2006-06-02
Latest Date of Registration : 2010-03-23
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PharmaCompass offers a list of GUANIDINE HYDROCHLORIDE API 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 GUANIDINE HYDROCHLORIDE API manufacturer or GUANIDINE HYDROCHLORIDE API supplier for your needs.
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A Hydrochloride, Guanidine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Hydrochloride, Guanidine, including repackagers and relabelers. The FDA regulates Hydrochloride, Guanidine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Hydrochloride, Guanidine 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 Hydrochloride, Guanidine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Hydrochloride, Guanidine supplier is an individual or a company that provides Hydrochloride, Guanidine active pharmaceutical ingredient (API) or Hydrochloride, Guanidine finished formulations upon request. The Hydrochloride, Guanidine suppliers may include Hydrochloride, Guanidine API manufacturers, exporters, distributors and traders.
click here to find a list of Hydrochloride, Guanidine 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 Hydrochloride, Guanidine Drug Master File in Japan (Hydrochloride, Guanidine JDMF) empowers Hydrochloride, Guanidine 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 Hydrochloride, Guanidine JDMF during the approval evaluation for pharmaceutical products. At the time of Hydrochloride, Guanidine 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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