01 2Toyama Pharmaceutical Co., Ltd.
01 1Boric acid
02 1Boric acid (powder)
01 2Japan
Registration Number : 218MF10743
Registrant's Address : Kyodo Building, 1-2-6 Nihonbashi Honcho, Chuo-ku, Tokyo (Honcho)
Initial Date of Registration : 2006-09-06
Latest Date of Registration : 2006-09-06
Registration Number : 218MF10544
Registrant's Address : Kyodo Building, 1-2-6 Nihonbashi Honcho, Chuo-ku, Tokyo (Honcho)
Initial Date of Registration : 2006-06-01
Latest Date of Registration : 2006-06-01
A Boric Acid manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Boric Acid, including repackagers and relabelers. The FDA regulates Boric Acid manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Boric Acid 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 Boric Acid manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Boric Acid supplier is an individual or a company that provides Boric Acid active pharmaceutical ingredient (API) or Boric Acid finished formulations upon request. The Boric Acid suppliers may include Boric Acid API manufacturers, exporters, distributors and traders.
click here to find a list of Boric Acid 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 Boric Acid Drug Master File in Japan (Boric Acid JDMF) empowers Boric Acid 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 Boric Acid JDMF during the approval evaluation for pharmaceutical products. At the time of Boric Acid 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 Boric Acid suppliers with JDMF on PharmaCompass.
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