01 1Orgapharm
01 1Dong-A ST Co., Ltd.
01 1Imiquimode
01 1Egypt
Registrant Name : Dong-A ST Co., Ltd.
Registration Date : 2023-02-15
Registration Number : 20230215-209-J-1446
Manufacturer Name : Orgapharm
Manufacturer Address : Zone Industrielle, Rue du Moulin De La Canne, Pithiviers, 45300, France
A Imiquimod manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Imiquimod, including repackagers and relabelers. The FDA regulates Imiquimod manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Imiquimod 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 Imiquimod manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Imiquimod supplier is an individual or a company that provides Imiquimod active pharmaceutical ingredient (API) or Imiquimod finished formulations upon request. The Imiquimod suppliers may include Imiquimod API manufacturers, exporters, distributors and traders.
click here to find a list of Imiquimod 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 Imiquimod Drug Master File in Korea (Imiquimod KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Imiquimod. The MFDS reviews the Imiquimod KDMF as part of the drug registration process and uses the information provided in the Imiquimod KDMF to evaluate the safety and efficacy of the drug.
After submitting a Imiquimod 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 Imiquimod API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Imiquimod suppliers with KDMF on PharmaCompass.
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