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.
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A Boron sodium oxide (B4Na2O7) manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Boron sodium oxide (B4Na2O7), including repackagers and relabelers. The FDA regulates Boron sodium oxide (B4Na2O7) manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Boron sodium oxide (B4Na2O7) 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 Boron sodium oxide (B4Na2O7) supplier is an individual or a company that provides Boron sodium oxide (B4Na2O7) active pharmaceutical ingredient (API) or Boron sodium oxide (B4Na2O7) finished formulations upon request. The Boron sodium oxide (B4Na2O7) suppliers may include Boron sodium oxide (B4Na2O7) API manufacturers, exporters, distributors and traders.
click here to find a list of Boron sodium oxide (B4Na2O7) 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 Boron sodium oxide (B4Na2O7) Drug Master File in Japan (Boron sodium oxide (B4Na2O7) JDMF) empowers Boron sodium oxide (B4Na2O7) 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 Boron sodium oxide (B4Na2O7) JDMF during the approval evaluation for pharmaceutical products. At the time of Boron sodium oxide (B4Na2O7) 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 Boron sodium oxide (B4Na2O7) suppliers with JDMF on PharmaCompass.
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