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.
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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 RTR-024058 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of RTR-024058, including repackagers and relabelers. The FDA regulates RTR-024058 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. RTR-024058 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 RTR-024058 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A RTR-024058 supplier is an individual or a company that provides RTR-024058 active pharmaceutical ingredient (API) or RTR-024058 finished formulations upon request. The RTR-024058 suppliers may include RTR-024058 API manufacturers, exporters, distributors and traders.
click here to find a list of RTR-024058 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 RTR-024058 Drug Master File in Japan (RTR-024058 JDMF) empowers RTR-024058 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 RTR-024058 JDMF during the approval evaluation for pharmaceutical products. At the time of RTR-024058 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 RTR-024058 suppliers with JDMF on PharmaCompass.
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