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