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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 Diovan manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Diovan, including repackagers and relabelers. The FDA regulates Diovan manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Diovan 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 Diovan manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Diovan supplier is an individual or a company that provides Diovan active pharmaceutical ingredient (API) or Diovan finished formulations upon request. The Diovan suppliers may include Diovan API manufacturers, exporters, distributors and traders.
click here to find a list of Diovan suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a Diovan Drug Master File in Korea (Diovan KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Diovan. The MFDS reviews the Diovan KDMF as part of the drug registration process and uses the information provided in the Diovan KDMF to evaluate the safety and efficacy of the drug.
After submitting a Diovan KDMF to the MFDS, the registered manufacturer can provide importers or distributors with the registration number without revealing confidential information to Korean business partners. Applicants seeking to register their Diovan API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Diovan suppliers with KDMF on PharmaCompass.
We have 31 companies offering Diovan
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