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01 Zhejiang Shenzhou Pharmaceutical Co. , Ltd. (2)
01 Canrenoate potassium (1)
02 Potassium Canrenoate (1)
01 China (2)
80
PharmaCompass offers a list of Canrenoate Potassium 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 Canrenoate Potassium manufacturer or Canrenoate Potassium supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Canrenoate Potassium manufacturer or Canrenoate Potassium supplier.
PharmaCompass also assists you with knowing the Canrenoate Potassium API Price utilized in the formulation of products. Canrenoate Potassium API Price is not always fixed or binding as the Canrenoate Potassium Price is obtained through a variety of data sources. The Canrenoate Potassium Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Canrenone manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Canrenone, including repackagers and relabelers. The FDA regulates Canrenone manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Canrenone 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 Canrenone manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Canrenone supplier is an individual or a company that provides Canrenone active pharmaceutical ingredient (API) or Canrenone finished formulations upon request. The Canrenone suppliers may include Canrenone API manufacturers, exporters, distributors and traders.
click here to find a list of Canrenone 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 Canrenone Drug Master File in Japan (Canrenone JDMF) empowers Canrenone 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 Canrenone JDMF during the approval evaluation for pharmaceutical products. At the time of Canrenone 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 Canrenone suppliers with JDMF on PharmaCompass.
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