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 Acetazolamide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Acetazolamide, including repackagers and relabelers. The FDA regulates Acetazolamide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Acetazolamide 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 Acetazolamide manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Acetazolamide supplier is an individual or a company that provides Acetazolamide active pharmaceutical ingredient (API) or Acetazolamide finished formulations upon request. The Acetazolamide suppliers may include Acetazolamide API manufacturers, exporters, distributors and traders.
click here to find a list of Acetazolamide 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 Acetazolamide Drug Master File in Korea (Acetazolamide KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Acetazolamide. The MFDS reviews the Acetazolamide KDMF as part of the drug registration process and uses the information provided in the Acetazolamide KDMF to evaluate the safety and efficacy of the drug.
After submitting a Acetazolamide 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 Acetazolamide API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Acetazolamide suppliers with KDMF on PharmaCompass.
We have 1 companies offering Acetazolamide
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