01 1Bihoku Powder Industry Co., Ltd.
01 1Japanese Pharmacopoeia precipitated calcium carbonate (production only)
01 1Japan
"Japanese Pharmacopoeia Precipitated Calcium Carbonate" (for manufacturing only)
Registration Number : 217MF10309
Registrant's Address : 704 Nishikata, Niimi City, Okayama Prefecture
Initial Date of Registration : 2005-07-11
Latest Date of Registration : 2006-11-15
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PharmaCompass offers a list of Calcium Carbonate 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 Calcium Carbonate manufacturer or Calcium Carbonate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Calcium Carbonate manufacturer or Calcium Carbonate supplier.
PharmaCompass also assists you with knowing the Calcium Carbonate API Price utilized in the formulation of products. Calcium Carbonate API Price is not always fixed or binding as the Calcium Carbonate Price is obtained through a variety of data sources. The Calcium Carbonate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A E170 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of E170, including repackagers and relabelers. The FDA regulates E170 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. E170 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 E170 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A E170 supplier is an individual or a company that provides E170 active pharmaceutical ingredient (API) or E170 finished formulations upon request. The E170 suppliers may include E170 API manufacturers, exporters, distributors and traders.
click here to find a list of E170 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 E170 Drug Master File in Japan (E170 JDMF) empowers E170 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 E170 JDMF during the approval evaluation for pharmaceutical products. At the time of E170 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 E170 suppliers with JDMF on PharmaCompass.
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