01 1Tokiwa Phytochemical Laboratory Co., Ltd.
01 1Sen Roh side calcium 60%
01 1Japan
Registration Number : 226MF10108
Registrant's Address : 158 Kinoko, Sakura City, Chiba Prefecture
Initial Date of Registration : 2014-05-26
Latest Date of Registration : 2014-05-26
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PharmaCompass offers a list of Calcium 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 manufacturer or Calcium supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Calcium manufacturer or Calcium supplier.
PharmaCompass also assists you with knowing the Calcium API Price utilized in the formulation of products. Calcium API Price is not always fixed or binding as the Calcium Price is obtained through a variety of data sources. The Calcium Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Calcium manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Calcium, including repackagers and relabelers. The FDA regulates Calcium manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Calcium 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 Calcium supplier is an individual or a company that provides Calcium active pharmaceutical ingredient (API) or Calcium finished formulations upon request. The Calcium suppliers may include Calcium API manufacturers, exporters, distributors and traders.
click here to find a list of Calcium 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 Calcium Drug Master File in Japan (Calcium JDMF) empowers Calcium 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 Calcium JDMF during the approval evaluation for pharmaceutical products. At the time of Calcium 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 Calcium suppliers with JDMF on PharmaCompass.
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