01 1ROQUETTE FRERES
01 1Rocket Korea Ltd.
01 1Icodextrin
01 1France
Registrant Name : Rocket Korea Ltd.
Registration Date : 2024-08-28
Registration Number : 20240828-211-J-1682
Manufacturer Name : ROQUETTE FRERES
Manufacturer Address : 1 Rue de la Haute Loge, 62136 LESTREM, France
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PharmaCompass offers a list of Icodextrin 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 Icodextrin manufacturer or Icodextrin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Icodextrin manufacturer or Icodextrin supplier.
PharmaCompass also assists you with knowing the Icodextrin API Price utilized in the formulation of products. Icodextrin API Price is not always fixed or binding as the Icodextrin Price is obtained through a variety of data sources. The Icodextrin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A NCGC00024846-08 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of NCGC00024846-08, including repackagers and relabelers. The FDA regulates NCGC00024846-08 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. NCGC00024846-08 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 NCGC00024846-08 supplier is an individual or a company that provides NCGC00024846-08 active pharmaceutical ingredient (API) or NCGC00024846-08 finished formulations upon request. The NCGC00024846-08 suppliers may include NCGC00024846-08 API manufacturers, exporters, distributors and traders.
click here to find a list of NCGC00024846-08 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 NCGC00024846-08 Drug Master File in Korea (NCGC00024846-08 KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of NCGC00024846-08. The MFDS reviews the NCGC00024846-08 KDMF as part of the drug registration process and uses the information provided in the NCGC00024846-08 KDMF to evaluate the safety and efficacy of the drug.
After submitting a NCGC00024846-08 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 NCGC00024846-08 API can apply through the Korea Drug Master File (KDMF).
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