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