01 1ROVI ESCÚZAR, SL
01 1Ilsung IS Co., Ltd.
01 1Bemiparin sodium
01 1Blank
Registrant Name : Ilsung IS Co., Ltd.
Registration Date : 2025-02-21
Registration Number : 20250221-211-J-1761
Manufacturer Name : ROVI ESCÚZAR, SL
Manufacturer Address : Avenida de la Serrezuela, 5518130 ESCÚZAR (GRANADA), SPAIN
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A Heparin sodium 25,000 units in dextrose 5% in plastic container manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Heparin sodium 25,000 units in dextrose 5% in plastic container, including repackagers and relabelers. The FDA regulates Heparin sodium 25,000 units in dextrose 5% in plastic container manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Heparin sodium 25,000 units in dextrose 5% in plastic container 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 Heparin sodium 25,000 units in dextrose 5% in plastic container supplier is an individual or a company that provides Heparin sodium 25,000 units in dextrose 5% in plastic container active pharmaceutical ingredient (API) or Heparin sodium 25,000 units in dextrose 5% in plastic container finished formulations upon request. The Heparin sodium 25,000 units in dextrose 5% in plastic container suppliers may include Heparin sodium 25,000 units in dextrose 5% in plastic container 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 Heparin sodium 25,000 units in dextrose 5% in plastic container Drug Master File in Korea (Heparin sodium 25,000 units in dextrose 5% in plastic container KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Heparin sodium 25,000 units in dextrose 5% in plastic container. The MFDS reviews the Heparin sodium 25,000 units in dextrose 5% in plastic container KDMF as part of the drug registration process and uses the information provided in the Heparin sodium 25,000 units in dextrose 5% in plastic container KDMF to evaluate the safety and efficacy of the drug.
After submitting a Heparin sodium 25,000 units in dextrose 5% in plastic container 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 Heparin sodium 25,000 units in dextrose 5% in plastic container API can apply through the Korea Drug Master File (KDMF).
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