01 1Mitsubishi Tanabe Pharma Factory, Ltd.
01 1Ebokaruseto
01 1Japan
Registration Number : 229MF10027
Registrant's Address : 2-10 Doshomachi 3-chome, Chuo-ku, Osaka City, Osaka Prefecture
Initial Date of Registration : 2017-02-08
Latest Date of Registration : 2017-12-25
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PharmaCompass offers a list of Evocalcet 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 Evocalcet manufacturer or Evocalcet supplier for your needs.
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PharmaCompass also assists you with knowing the Evocalcet API Price utilized in the formulation of products. Evocalcet API Price is not always fixed or binding as the Evocalcet Price is obtained through a variety of data sources. The Evocalcet Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A 870964-67-3 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 870964-67-3, including repackagers and relabelers. The FDA regulates 870964-67-3 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 870964-67-3 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 870964-67-3 supplier is an individual or a company that provides 870964-67-3 active pharmaceutical ingredient (API) or 870964-67-3 finished formulations upon request. The 870964-67-3 suppliers may include 870964-67-3 API manufacturers, exporters, distributors and traders.
click here to find a list of 870964-67-3 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 870964-67-3 Drug Master File in Japan (870964-67-3 JDMF) empowers 870964-67-3 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 870964-67-3 JDMF during the approval evaluation for pharmaceutical products. At the time of 870964-67-3 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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