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 Liquaemin sodium preservative free manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Liquaemin sodium preservative free, including repackagers and relabelers. The FDA regulates Liquaemin sodium preservative free manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Liquaemin sodium preservative free 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 Liquaemin sodium preservative free supplier is an individual or a company that provides Liquaemin sodium preservative free active pharmaceutical ingredient (API) or Liquaemin sodium preservative free finished formulations upon request. The Liquaemin sodium preservative free suppliers may include Liquaemin sodium preservative free 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 Liquaemin sodium preservative free Drug Master File in Korea (Liquaemin sodium preservative free KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Liquaemin sodium preservative free. The MFDS reviews the Liquaemin sodium preservative free KDMF as part of the drug registration process and uses the information provided in the Liquaemin sodium preservative free KDMF to evaluate the safety and efficacy of the drug.
After submitting a Liquaemin sodium preservative free 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 Liquaemin sodium preservative free API can apply through the Korea Drug Master File (KDMF).
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