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PharmaCompass offers a list of Diosmin 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 Diosmin manufacturer or Diosmin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Diosmin manufacturer or Diosmin supplier.
PharmaCompass also assists you with knowing the Diosmin API Price utilized in the formulation of products. Diosmin API Price is not always fixed or binding as the Diosmin Price is obtained through a variety of data sources. The Diosmin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Diosmin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Diosmin, including repackagers and relabelers. The FDA regulates Diosmin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Diosmin 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 Diosmin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Diosmin supplier is an individual or a company that provides Diosmin active pharmaceutical ingredient (API) or Diosmin finished formulations upon request. The Diosmin suppliers may include Diosmin API manufacturers, exporters, distributors and traders.
click here to find a list of Diosmin 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 Diosmin Drug Master File in Korea (Diosmin KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Diosmin. The MFDS reviews the Diosmin KDMF as part of the drug registration process and uses the information provided in the Diosmin KDMF to evaluate the safety and efficacy of the drug.
After submitting a Diosmin 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 Diosmin API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Diosmin suppliers with KDMF on PharmaCompass.
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