01 1Olon SPA
01 1DKS Korea Co., Ltd.
01 1Mefloquine hydrochloride
01 1Italy
Registrant Name : DKS Korea Co., Ltd.
Registration Date : 2022-09-28
Registration Number : 20220928-209-J-1371
Manufacturer Name : Olon SPA
Manufacturer Address : VIA LIVELLI, 1(loc. FRAZIONE MAIRANO) - 26852 CASALETTO LODIGIANO (LO), Italy
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PharmaCompass offers a list of Mefloquine 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 Mefloquine manufacturer or Mefloquine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Mefloquine manufacturer or Mefloquine supplier.
PharmaCompass also assists you with knowing the Mefloquine API Price utilized in the formulation of products. Mefloquine API Price is not always fixed or binding as the Mefloquine Price is obtained through a variety of data sources. The Mefloquine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A MQ manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of MQ, including repackagers and relabelers. The FDA regulates MQ manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. MQ 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 MQ manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A MQ supplier is an individual or a company that provides MQ active pharmaceutical ingredient (API) or MQ finished formulations upon request. The MQ suppliers may include MQ API manufacturers, exporters, distributors and traders.
click here to find a list of MQ 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 MQ Drug Master File in Korea (MQ KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of MQ. The MFDS reviews the MQ KDMF as part of the drug registration process and uses the information provided in the MQ KDMF to evaluate the safety and efficacy of the drug.
After submitting a MQ 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 MQ API can apply through the Korea Drug Master File (KDMF).
click here to find a list of MQ suppliers with KDMF on PharmaCompass.
