01 1Cerbios Pharma SA@[Spray Drying Plant] Micro-Sphere SA
01 1MediHelpline Co., Ltd.
01 1Tiotropium bromide
01 1Switzerland
Registrant Name : MediHelpline Co., Ltd.
Registration Date : 2019-08-01
Registration Number : 20190801-211-J-399
Manufacturer Name : Cerbios Pharma SA@[Spray Dry...
Manufacturer Address : Via Figino 6, 6917 Barbengo, Switzerland@[Spray drying factory]Via Cantonale 77, 6998...
A Tiotropium Bromide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tiotropium Bromide, including repackagers and relabelers. The FDA regulates Tiotropium Bromide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tiotropium Bromide 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 Tiotropium Bromide manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Tiotropium Bromide supplier is an individual or a company that provides Tiotropium Bromide active pharmaceutical ingredient (API) or Tiotropium Bromide finished formulations upon request. The Tiotropium Bromide suppliers may include Tiotropium Bromide API manufacturers, exporters, distributors and traders.
click here to find a list of Tiotropium Bromide 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 Tiotropium Bromide Drug Master File in Korea (Tiotropium Bromide KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Tiotropium Bromide. The MFDS reviews the Tiotropium Bromide KDMF as part of the drug registration process and uses the information provided in the Tiotropium Bromide KDMF to evaluate the safety and efficacy of the drug.
After submitting a Tiotropium Bromide 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 Tiotropium Bromide API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Tiotropium Bromide suppliers with KDMF on PharmaCompass.
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