01 1PolyPeptide Laboratories (Sweden) AB
01 1Ferring Korea Co., Ltd.
01 1Degarelics
01 1Switzerland
Registrant Name : Ferring Korea Co., Ltd.
Registration Date : 2013-03-18
Registration Number : Su3127-1-ND
Manufacturer Name : PolyPeptide Laboratories (Sw...
Manufacturer Address : Hogerudsgatan 21 SE-216 13 Limhamn
15
PharmaCompass offers a list of Degarelix Acetate API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Degarelix Acetate manufacturer or Degarelix Acetate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Degarelix Acetate manufacturer or Degarelix Acetate supplier.
A Degarelix Acetate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Degarelix Acetate, including repackagers and relabelers. The FDA regulates Degarelix Acetate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Degarelix Acetate 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 Degarelix Acetate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Degarelix Acetate supplier is an individual or a company that provides Degarelix Acetate active pharmaceutical ingredient (API) or Degarelix Acetate finished formulations upon request. The Degarelix Acetate suppliers may include Degarelix Acetate API manufacturers, exporters, distributors and traders.
click here to find a list of Degarelix Acetate suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA 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 Degarelix Acetate Drug Master File in Korea (Degarelix Acetate KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Degarelix Acetate. The MFDS reviews the Degarelix Acetate KDMF as part of the drug registration process and uses the information provided in the Degarelix Acetate KDMF to evaluate the safety and efficacy of the drug.
After submitting a Degarelix Acetate 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 Degarelix Acetate API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Degarelix Acetate suppliers with KDMF on PharmaCompass.
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