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