01 2Toyama Pharmaceutical Co., Ltd.
01 1Japanese Pharmacopoeia borax (powder) (production only)
02 1Japanese Pharmacopoeia borax (production only)
01 2Japan
Japanese Pharmacopoeia Borax (for manufacturing only)
Registration Number : 219MF10069
Registrant's Address : Kyodo Building, 1-2-6 Honmachi, Nihonbashi, Chuo-ku, Tokyo (Honmachi)
Initial Date of Registration : 2007-03-05
Latest Date of Registration : 2007-03-05
Japanese Pharmacopoeia Borax (powder) (for manufacturing only)
Registration Number : 219MF10068
Registrant's Address : Kyodo Building, 1-2-6 Honmachi, Nihonbashi, Chuo-ku, Tokyo (Honmachi)
Initial Date of Registration : 2007-03-05
Latest Date of Registration : 2007-03-05
A Borax Solution manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Borax Solution, including repackagers and relabelers. The FDA regulates Borax Solution manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Borax Solution 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 Borax Solution supplier is an individual or a company that provides Borax Solution active pharmaceutical ingredient (API) or Borax Solution finished formulations upon request. The Borax Solution suppliers may include Borax Solution API manufacturers, exporters, distributors and traders.
click here to find a list of Borax Solution 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 Borax Solution Drug Master File in Japan (Borax Solution JDMF) empowers Borax Solution 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 Borax Solution JDMF during the approval evaluation for pharmaceutical products. At the time of Borax Solution 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 Borax Solution suppliers with JDMF on PharmaCompass.
We have 1 companies offering Borax Solution
Get in contact with the supplier of your choice:
LOOKING FOR A SUPPLIER?
