01 1PolyPeptide Laboratories (Sweden) AB
01 1Korea Ferring Pharmaceutical Co., Ltd.
01 1Degarelix
01 1Switzerland
Registrant Name : Korea Ferring Pharmaceutical 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
99
PharmaCompass offers a list of Degarelix Acetate 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 Degarelix Acetate manufacturer or Degarelix Acetate supplier for your needs.
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PharmaCompass also assists you with knowing the Degarelix Acetate API Price utilized in the formulation of products. Degarelix Acetate API Price is not always fixed or binding as the Degarelix Acetate Price is obtained through a variety of data sources. The Degarelix Acetate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A 934016-19-0 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 934016-19-0, including repackagers and relabelers. The FDA regulates 934016-19-0 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 934016-19-0 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A 934016-19-0 supplier is an individual or a company that provides 934016-19-0 active pharmaceutical ingredient (API) or 934016-19-0 finished formulations upon request. The 934016-19-0 suppliers may include 934016-19-0 API manufacturers, exporters, distributors and traders.
click here to find a list of 934016-19-0 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 934016-19-0 Drug Master File in Korea (934016-19-0 KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of 934016-19-0. The MFDS reviews the 934016-19-0 KDMF as part of the drug registration process and uses the information provided in the 934016-19-0 KDMF to evaluate the safety and efficacy of the drug.
After submitting a 934016-19-0 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 934016-19-0 API can apply through the Korea Drug Master File (KDMF).
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