01 1Bayer AG@Bayer AG
01 1Bayer Korea Co., Ltd.
01 1Cyproterone acetate
01 1Germany
Registrant Name : Bayer Korea Co., Ltd.
Registration Date : 2021-08-10
Registration Number : 20210810-209-J-1087
Manufacturer Name : Bayer AG@Bayer AG
Manufacturer Address : Ernst-Schering-Straβe 14, 59192 Bergkamen, Germany@Max-Dohrn-Straβe 8, Drug Substan...
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PharmaCompass offers a list of Cyproterone 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 Cyproterone Acetate manufacturer or Cyproterone Acetate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Cyproterone Acetate manufacturer or Cyproterone Acetate supplier.
A Cyprostat® manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cyprostat®, including repackagers and relabelers. The FDA regulates Cyprostat® manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cyprostat® 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 Cyprostat® manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Cyprostat® supplier is an individual or a company that provides Cyprostat® active pharmaceutical ingredient (API) or Cyprostat® finished formulations upon request. The Cyprostat® suppliers may include Cyprostat® API manufacturers, exporters, distributors and traders.
click here to find a list of Cyprostat® 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 Cyprostat® Drug Master File in Korea (Cyprostat® KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Cyprostat®. The MFDS reviews the Cyprostat® KDMF as part of the drug registration process and uses the information provided in the Cyprostat® KDMF to evaluate the safety and efficacy of the drug.
After submitting a Cyprostat® 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 Cyprostat® API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Cyprostat® suppliers with KDMF on PharmaCompass.
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