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...
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PharmaCompass offers a list of Tiotropium Bromide API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Tiotropium Bromide manufacturer or Tiotropium Bromide supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Tiotropium Bromide manufacturer or Tiotropium Bromide supplier.
PharmaCompass also assists you with knowing the Tiotropium Bromide API Price utilized in the formulation of products. Tiotropium Bromide API Price is not always fixed or binding as the Tiotropium Bromide Price is obtained through a variety of data sources. The Tiotropium Bromide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A SPIRIVA manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of SPIRIVA, including repackagers and relabelers. The FDA regulates SPIRIVA manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. SPIRIVA 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 SPIRIVA manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A SPIRIVA supplier is an individual or a company that provides SPIRIVA active pharmaceutical ingredient (API) or SPIRIVA finished formulations upon request. The SPIRIVA suppliers may include SPIRIVA API manufacturers, exporters, distributors and traders.
click here to find a list of SPIRIVA 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 SPIRIVA Drug Master File in Korea (SPIRIVA KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of SPIRIVA. The MFDS reviews the SPIRIVA KDMF as part of the drug registration process and uses the information provided in the SPIRIVA KDMF to evaluate the safety and efficacy of the drug.
After submitting a SPIRIVA 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 SPIRIVA API can apply through the Korea Drug Master File (KDMF).
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