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01 1ROVI ESCÚZAR, SL
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01 1Ilsung IS Co., Ltd.
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01 1Bemiparin sodium
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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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PharmaCompass offers a list of Dalteparin sodium 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 Dalteparin sodium manufacturer or Dalteparin sodium supplier for your needs.
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A Lipo-hepin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Lipo-hepin, including repackagers and relabelers. The FDA regulates Lipo-hepin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Lipo-hepin 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 Lipo-hepin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Lipo-hepin supplier is an individual or a company that provides Lipo-hepin active pharmaceutical ingredient (API) or Lipo-hepin finished formulations upon request. The Lipo-hepin suppliers may include Lipo-hepin API manufacturers, exporters, distributors and traders.
click here to find a list of Lipo-hepin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price 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 Lipo-hepin Drug Master File in Korea (Lipo-hepin KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Lipo-hepin. The MFDS reviews the Lipo-hepin KDMF as part of the drug registration process and uses the information provided in the Lipo-hepin KDMF to evaluate the safety and efficacy of the drug.
After submitting a Lipo-hepin 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 Lipo-hepin API can apply through the Korea Drug Master File (KDMF).
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