01 1Roquette Freres
01 1Rocket Korea Ltd.
01 1Glucose monohydrate
01 1France
Registrant Name : Rocket Korea Ltd.
Registration Date : 2024-12-23
Registration Number : 20241223-211-J-1734
Manufacturer Name : Roquette Freres
Manufacturer Address : 1 Rue de la Haute Loge, 62136 LESTREM, France
36
PharmaCompass offers a list of Dextrose Monohydrate API 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 Dextrose Monohydrate API manufacturer or Dextrose Monohydrate API supplier for your needs.
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PharmaCompass also assists you with knowing the Dextrose Monohydrate API API Price utilized in the formulation of products. Dextrose Monohydrate API API Price is not always fixed or binding as the Dextrose Monohydrate API Price is obtained through a variety of data sources. The Dextrose Monohydrate API Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A C6H12O6.H2O manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of C6H12O6.H2O, including repackagers and relabelers. The FDA regulates C6H12O6.H2O manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. C6H12O6.H2O 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 C6H12O6.H2O supplier is an individual or a company that provides C6H12O6.H2O active pharmaceutical ingredient (API) or C6H12O6.H2O finished formulations upon request. The C6H12O6.H2O suppliers may include C6H12O6.H2O 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 C6H12O6.H2O Drug Master File in Korea (C6H12O6.H2O KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of C6H12O6.H2O. The MFDS reviews the C6H12O6.H2O KDMF as part of the drug registration process and uses the information provided in the C6H12O6.H2O KDMF to evaluate the safety and efficacy of the drug.
After submitting a C6H12O6.H2O 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 C6H12O6.H2O API can apply through the Korea Drug Master File (KDMF).
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