01 1Tomita Pharmaceutical Co., Ltd.
01 1Manganese Chloride
01 1Japan
Registration Number : 302MF10057
Registrant's Address : Tokushima Prefecture Naruto City Setocho Myojin Maruyama 85-1
Initial Date of Registration : 2020-05-12
Latest Date of Registration : 2020-05-12
A manganese chloride, hexahydrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of manganese chloride, hexahydrate, including repackagers and relabelers. The FDA regulates manganese chloride, hexahydrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. manganese chloride, hexahydrate API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A manganese chloride, hexahydrate supplier is an individual or a company that provides manganese chloride, hexahydrate active pharmaceutical ingredient (API) or manganese chloride, hexahydrate finished formulations upon request. The manganese chloride, hexahydrate suppliers may include manganese chloride, hexahydrate API manufacturers, exporters, distributors and traders.
click here to find a list of manganese chloride, hexahydrate 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 manganese chloride, hexahydrate Drug Master File in Japan (manganese chloride, hexahydrate JDMF) empowers manganese chloride, hexahydrate 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 manganese chloride, hexahydrate JDMF during the approval evaluation for pharmaceutical products. At the time of manganese chloride, hexahydrate 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 manganese chloride, hexahydrate suppliers with JDMF on PharmaCompass.
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