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PharmaCompass offers a list of Valsartan 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 Valsartan manufacturer or Valsartan supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Valsartan manufacturer or Valsartan supplier.
PharmaCompass also assists you with knowing the Valsartan API Price utilized in the formulation of products. Valsartan API Price is not always fixed or binding as the Valsartan Price is obtained through a variety of data sources. The Valsartan Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Valsartan manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Valsartan, including repackagers and relabelers. The FDA regulates Valsartan manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Valsartan 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 Valsartan manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Valsartan supplier is an individual or a company that provides Valsartan active pharmaceutical ingredient (API) or Valsartan finished formulations upon request. The Valsartan suppliers may include Valsartan API manufacturers, exporters, distributors and traders.
click here to find a list of Valsartan 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 Valsartan Drug Master File in Japan (Valsartan JDMF) empowers Valsartan 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 Valsartan JDMF during the approval evaluation for pharmaceutical products. At the time of Valsartan 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 Valsartan suppliers with JDMF on PharmaCompass.
We have 16 companies offering Valsartan
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DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
