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
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PharmaCompass offers a list of Borax Solution API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Borax Solution manufacturer or Borax Solution supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Borax Solution manufacturer or Borax Solution supplier.
PharmaCompass also assists you with knowing the Borax Solution API Price utilized in the formulation of products. Borax Solution API Price is not always fixed or binding as the Borax Solution Price is obtained through a variety of data sources. The Borax Solution Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Komex manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Komex, including repackagers and relabelers. The FDA regulates Komex manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Komex 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 Komex supplier is an individual or a company that provides Komex active pharmaceutical ingredient (API) or Komex finished formulations upon request. The Komex suppliers may include Komex API manufacturers, exporters, distributors and traders.
click here to find a list of Komex 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 Komex Drug Master File in Japan (Komex JDMF) empowers Komex 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 Komex JDMF during the approval evaluation for pharmaceutical products. At the time of Komex 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 Komex suppliers with JDMF on PharmaCompass.
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