01 1Kyowa Chemical Industry Co., Ltd.
01 1Japanese Pharmacopoeia calcium hydrogen phosphate hydrate (manufactured only)
01 1Japan
Japanese Pharmacopoeia Calcium Hydrogen Phosphate Hydrate (For manufacturing purposes only)
Registration Number : 221MF10072
Registrant's Address : 305 Yashima Nishimachi, Takamatsu City, Kagawa Prefecture
Initial Date of Registration : 2009-04-08
Latest Date of Registration : 2009-04-08
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PharmaCompass offers a list of Dibasic Calcium Phosphate Dihydrate 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 Dibasic Calcium Phosphate Dihydrate manufacturer or Dibasic Calcium Phosphate Dihydrate supplier for your needs.
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PharmaCompass also assists you with knowing the Dibasic Calcium Phosphate Dihydrate API Price utilized in the formulation of products. Dibasic Calcium Phosphate Dihydrate API Price is not always fixed or binding as the Dibasic Calcium Phosphate Dihydrate Price is obtained through a variety of data sources. The Dibasic Calcium Phosphate Dihydrate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A 04231_RIEDEL manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 04231_RIEDEL, including repackagers and relabelers. The FDA regulates 04231_RIEDEL manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 04231_RIEDEL API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A 04231_RIEDEL supplier is an individual or a company that provides 04231_RIEDEL active pharmaceutical ingredient (API) or 04231_RIEDEL finished formulations upon request. The 04231_RIEDEL suppliers may include 04231_RIEDEL API manufacturers, exporters, distributors and traders.
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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 04231_RIEDEL Drug Master File in Japan (04231_RIEDEL JDMF) empowers 04231_RIEDEL 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 04231_RIEDEL JDMF during the approval evaluation for pharmaceutical products. At the time of 04231_RIEDEL JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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