01 1Mitsubishi Tanabe Pharma Factory, Ltd.
01 1Ebokaruseto
01 1Japan
Registration Number : 229MF10027
Registrant's Address : Osaka Prefecture, Osaka City, Chuo Ward, Doshomachi 3-2-10
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.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Evocalcet manufacturer or Evocalcet supplier.
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 KHK-7580 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of KHK-7580, including repackagers and relabelers. The FDA regulates KHK-7580 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. KHK-7580 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 KHK-7580 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A KHK-7580 supplier is an individual or a company that provides KHK-7580 active pharmaceutical ingredient (API) or KHK-7580 finished formulations upon request. The KHK-7580 suppliers may include KHK-7580 API manufacturers, exporters, distributors and traders.
click here to find a list of KHK-7580 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 KHK-7580 Drug Master File in Japan (KHK-7580 JDMF) empowers KHK-7580 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 KHK-7580 JDMF during the approval evaluation for pharmaceutical products. At the time of KHK-7580 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 KHK-7580 suppliers with JDMF on PharmaCompass.
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