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