01 1Shizuoka Caffeine Industry Co., Ltd.
01 1Japanese Pharmacopoeia chlorphenesin carbamate (production only)
01 1Japan
Japanese Pharmacopoeia Chlorphenesin Carbamate (for manufacturing only)
Registration Number : 217MF10607
Registrant's Address : 129 Suidocho, Aoi Ward, Shizuoka City, Shizuoka Prefecture
Initial Date of Registration : 2005-09-14
Latest Date of Registration : 2008-02-25
A Chlorphenesin Carbamate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Chlorphenesin Carbamate, including repackagers and relabelers. The FDA regulates Chlorphenesin Carbamate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Chlorphenesin Carbamate 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 Chlorphenesin Carbamate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Chlorphenesin Carbamate supplier is an individual or a company that provides Chlorphenesin Carbamate active pharmaceutical ingredient (API) or Chlorphenesin Carbamate finished formulations upon request. The Chlorphenesin Carbamate suppliers may include Chlorphenesin Carbamate API manufacturers, exporters, distributors and traders.
click here to find a list of Chlorphenesin Carbamate 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 Chlorphenesin Carbamate Drug Master File in Japan (Chlorphenesin Carbamate JDMF) empowers Chlorphenesin Carbamate 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 Chlorphenesin Carbamate JDMF during the approval evaluation for pharmaceutical products. At the time of Chlorphenesin Carbamate 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 Chlorphenesin Carbamate suppliers with JDMF on PharmaCompass.
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