Polpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.
01 1Pharmaceutical Works Polpharma S.A.
01 1Wooshin Labotech Co., Ltd.
01 1Acetazolamide
01 1Poland
Polpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.
Registrant Name : Wooshin Labotech Co., Ltd.
Registration Date : 2020-10-19
Registration Number : 20201019-210-J-595
Manufacturer Name : Pharmaceutical Works Polphar...
Manufacturer Address : 19. Pelplinska Str, 83-200 Starogard Gdanski, Poland
A Carbinib manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Carbinib, including repackagers and relabelers. The FDA regulates Carbinib manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Carbinib 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 Carbinib manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Carbinib supplier is an individual or a company that provides Carbinib active pharmaceutical ingredient (API) or Carbinib finished formulations upon request. The Carbinib suppliers may include Carbinib API manufacturers, exporters, distributors and traders.
click here to find a list of Carbinib 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 Carbinib Drug Master File in Korea (Carbinib KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Carbinib. The MFDS reviews the Carbinib KDMF as part of the drug registration process and uses the information provided in the Carbinib KDMF to evaluate the safety and efficacy of the drug.
After submitting a Carbinib 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 Carbinib API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Carbinib suppliers with KDMF on PharmaCompass.
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