01 1YS Life Science Co., Ltd.
01 1YS Life Science Co., Ltd.
01 1Cabergolin
01 1South Korea
Registrant Name : YS Life Science Co., Ltd.
Registration Date : 2024-12-30
Registration Number : 20241230-211-J-1736
Manufacturer Name : YS Life Science Co., Ltd.
Manufacturer Address : 207 Sujeong-ro, Jangan-myeon, Hwaseong-si, Gyeonggi-do
83
PharmaCompass offers a list of Cabergoline 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 Cabergoline manufacturer or Cabergoline supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Cabergoline manufacturer or Cabergoline supplier.
A Cabaseril manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cabaseril, including repackagers and relabelers. The FDA regulates Cabaseril manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cabaseril 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 Cabaseril manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Cabaseril supplier is an individual or a company that provides Cabaseril active pharmaceutical ingredient (API) or Cabaseril finished formulations upon request. The Cabaseril suppliers may include Cabaseril API manufacturers, exporters, distributors and traders.
click here to find a list of Cabaseril 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 Cabaseril Drug Master File in Korea (Cabaseril KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Cabaseril. The MFDS reviews the Cabaseril KDMF as part of the drug registration process and uses the information provided in the Cabaseril KDMF to evaluate the safety and efficacy of the drug.
After submitting a Cabaseril 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 Cabaseril API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Cabaseril suppliers with KDMF on PharmaCompass.
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