01 1Ranke Quimica, SA@[Some process manufacturers] Ranke Quimica, SA (Planta Sant Celoni)@[Microprocess manufacturers] Catalent Micron Technologies Limited@[Microprocess manufacturers] Ranke Quimica, SA
01 1SPC Korea Co., Ltd.
01 1Aclidinium bromide
01 1Blank
Registrant Name : SPC Korea Co., Ltd.
Registration Date : 2014-06-30
Registration Number : Su4000-3-ND
Manufacturer Name : Ranke Quimica, SA@[Some proc...
Manufacturer Address : Carretera de Martorell 41-61, Sant Andreu de la Barca 08740 Barcelona, Spain@Ct...
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PharmaCompass offers a list of Aclidinium 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 Aclidinium Bromide manufacturer or Aclidinium Bromide supplier for your needs.
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A Eklira genuair (TN) manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Eklira genuair (TN), including repackagers and relabelers. The FDA regulates Eklira genuair (TN) manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Eklira genuair (TN) API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Eklira genuair (TN) supplier is an individual or a company that provides Eklira genuair (TN) active pharmaceutical ingredient (API) or Eklira genuair (TN) finished formulations upon request. The Eklira genuair (TN) suppliers may include Eklira genuair (TN) API manufacturers, exporters, distributors and traders.
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In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a Eklira genuair (TN) Drug Master File in Korea (Eklira genuair (TN) KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Eklira genuair (TN). The MFDS reviews the Eklira genuair (TN) KDMF as part of the drug registration process and uses the information provided in the Eklira genuair (TN) KDMF to evaluate the safety and efficacy of the drug.
After submitting a Eklira genuair (TN) 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 Eklira genuair (TN) API can apply through the Korea Drug Master File (KDMF).
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