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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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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PharmaCompass also assists you with knowing the Dalteparin sodium API Price utilized in the formulation of products. Dalteparin sodium API Price is not always fixed or binding as the Dalteparin sodium Price is obtained through a variety of data sources. The Dalteparin sodium Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Heparin, sodium salt manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Heparin, sodium salt, including repackagers and relabelers. The FDA regulates Heparin, sodium salt manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Heparin, sodium salt 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 salt supplier is an individual or a company that provides Heparin, sodium salt active pharmaceutical ingredient (API) or Heparin, sodium salt finished formulations upon request. The Heparin, sodium salt suppliers may include Heparin, sodium salt 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 salt Drug Master File in Korea (Heparin, sodium salt KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Heparin, sodium salt. The MFDS reviews the Heparin, sodium salt KDMF as part of the drug registration process and uses the information provided in the Heparin, sodium salt KDMF to evaluate the safety and efficacy of the drug.
After submitting a Heparin, sodium salt 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 salt API can apply through the Korea Drug Master File (KDMF).
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