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PharmaCompass offers a list of Sodium Valproate 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 Sodium Valproate manufacturer or Sodium Valproate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Sodium Valproate manufacturer or Sodium Valproate supplier.
PharmaCompass also assists you with knowing the Sodium Valproate API Price utilized in the formulation of products. Sodium Valproate API Price is not always fixed or binding as the Sodium Valproate Price is obtained through a variety of data sources. The Sodium Valproate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Sodium Valproate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sodium Valproate, including repackagers and relabelers. The FDA regulates Sodium Valproate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sodium Valproate 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 Sodium Valproate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Sodium Valproate supplier is an individual or a company that provides Sodium Valproate active pharmaceutical ingredient (API) or Sodium Valproate finished formulations upon request. The Sodium Valproate suppliers may include Sodium Valproate API manufacturers, exporters, distributors and traders.
click here to find a list of Sodium Valproate 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 Sodium Valproate Drug Master File in Korea (Sodium Valproate KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Sodium Valproate. The MFDS reviews the Sodium Valproate KDMF as part of the drug registration process and uses the information provided in the Sodium Valproate KDMF to evaluate the safety and efficacy of the drug.
After submitting a Sodium Valproate 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 Sodium Valproate API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Sodium Valproate suppliers with KDMF on PharmaCompass.
We have 3 companies offering Sodium Valproate
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EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
