01 1Kyowa Pharma Chemical Co., Ltd.
01 1Daiichi Sankyo Korea Co., Ltd.
01 1Philsicainide hydrochloride
01 1Japan
Registrant Name : Daiichi Sankyo Korea Co., Ltd.
Registration Date : 2007-05-21
Registration Number : 4937-1-ND
Manufacturer Name : Kyowa Pharma Chemical Co., L...
Manufacturer Address : 530, Chokeiji, Takaoka-city Toyama prefecture
89
PharmaCompass offers a list of Pilsicainide Hydrochloride 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 Pilsicainide Hydrochloride manufacturer or Pilsicainide Hydrochloride supplier for your needs.
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A 03C8I9296V manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 03C8I9296V, including repackagers and relabelers. The FDA regulates 03C8I9296V manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 03C8I9296V 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 03C8I9296V supplier is an individual or a company that provides 03C8I9296V active pharmaceutical ingredient (API) or 03C8I9296V finished formulations upon request. The 03C8I9296V suppliers may include 03C8I9296V 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 03C8I9296V Drug Master File in Korea (03C8I9296V KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of 03C8I9296V. The MFDS reviews the 03C8I9296V KDMF as part of the drug registration process and uses the information provided in the 03C8I9296V KDMF to evaluate the safety and efficacy of the drug.
After submitting a 03C8I9296V 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 03C8I9296V API can apply through the Korea Drug Master File (KDMF).
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