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