01 1Apotex pharmachem Inc
02 1Srini Pharmaceuticals Limited
01 2Repure Healthcare Co., Ltd.
01 2Deferifron
01 1Canada
02 1India
Registrant Name : Repure Healthcare Co., Ltd.
Registration Date : 2007-03-28
Registration Number : Su613-1-ND
Manufacturer Name : Apotex pharmachem Inc
Manufacturer Address : 11, 34, 50 Spalding Drive Brantford, Ontario N3T 6B8, Canada
Registrant Name : Repure Healthcare Co., Ltd.
Registration Date : 2012-06-15
Registration Number : Su613-2-ND
Manufacturer Name : Srini Pharmaceuticals Limite...
Manufacturer Address : Survey No. 247, Choutuppal-508 252 Nalgonda Distric Telangana State(TS), India
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PharmaCompass offers a list of Deferiprone 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 Deferiprone manufacturer or Deferiprone supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Deferiprone manufacturer or Deferiprone supplier.
A Ferriprox manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ferriprox, including repackagers and relabelers. The FDA regulates Ferriprox manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ferriprox 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 Ferriprox manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Ferriprox supplier is an individual or a company that provides Ferriprox active pharmaceutical ingredient (API) or Ferriprox finished formulations upon request. The Ferriprox suppliers may include Ferriprox API manufacturers, exporters, distributors and traders.
click here to find a list of Ferriprox 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 Ferriprox Drug Master File in Korea (Ferriprox KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Ferriprox. The MFDS reviews the Ferriprox KDMF as part of the drug registration process and uses the information provided in the Ferriprox KDMF to evaluate the safety and efficacy of the drug.
After submitting a Ferriprox 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 Ferriprox API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Ferriprox suppliers with KDMF on PharmaCompass.
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