Veranova: A CDMO that manages complexity with confidence.
01 2Macfarlan Smith Limited
02 1SpecGx LLC
01 1Baeksu Pharmaceutical Co., Ltd.
02 1Nosa Chemical Co., Ltd.
03 1Samung Industrial Co., Ltd.
01 3Sufentanil citrate
01 1Ireland
02 2U.S.A
Veranova: A CDMO that manages complexity with confidence.
Registrant Name : Samung Industrial Co., Ltd.
Registration Date : 2022-04-25
Registration Number : 20220421-210-J-1273(A)
Manufacturer Name : Macfarlan Smith Limited
Manufacturer Address : 10 Wheatfield Road, Edinburgh, EH11 2QA, United Kingdom
Veranova: A CDMO that manages complexity with confidence.
Registrant Name : Baeksu Pharmaceutical Co., Ltd.
Registration Date : 2022-04-21
Registration Number : 20220421-210-J-1273
Manufacturer Name : Macfarlan Smith Limited
Manufacturer Address : 10 Wheatfield Road, Edinburgh, EH11 2QA, United Kingdom
Registrant Name : Nosa Chemical Co., Ltd.
Registration Date : 2022-05-18
Registration Number : 20220518-210-J-1301
Manufacturer Name : SpecGx LLC
Manufacturer Address : 3600 North 2nd Street, St. Louis, MO 63147, USA
60
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 Sufenta Forte manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sufenta Forte, including repackagers and relabelers. The FDA regulates Sufenta Forte manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sufenta Forte 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 Sufenta Forte manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Sufenta Forte supplier is an individual or a company that provides Sufenta Forte active pharmaceutical ingredient (API) or Sufenta Forte finished formulations upon request. The Sufenta Forte suppliers may include Sufenta Forte API manufacturers, exporters, distributors and traders.
click here to find a list of Sufenta Forte 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 Sufenta Forte Drug Master File in Korea (Sufenta Forte KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Sufenta Forte. The MFDS reviews the Sufenta Forte KDMF as part of the drug registration process and uses the information provided in the Sufenta Forte KDMF to evaluate the safety and efficacy of the drug.
After submitting a Sufenta Forte 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 Sufenta Forte API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Sufenta Forte suppliers with KDMF on PharmaCompass.
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