Interquim comes from an international group of 50 companies active in the pharma, hospital, diagnostics, fine chemicals & feed sectors.
01 1Interquim, SA
01 1Bukwang Pharmaceutical Co., Ltd.
01 1Sertaconazole nitrate
01 1Spain
Interquim comes from an international group of 50 companies active in the pharma, hospital, diagnostics, fine chemicals & feed sectors.
Registrant Name : Bukwang Pharmaceutical Co., Ltd.
Registration Date : 2021-10-18
Registration Number : 20211018-209-J-1122
Manufacturer Name : Interquim, SA
Manufacturer Address : Joan Buscallà 10 E-08173 Sant Cugat del Vallès (Barcelona), Spain
100
PharmaCompass offers a list of Sertaconazole Nitrate 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 Sertaconazole Nitrate manufacturer or Sertaconazole Nitrate supplier for your needs.
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A Dermofix manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Dermofix, including repackagers and relabelers. The FDA regulates Dermofix manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Dermofix 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 Dermofix supplier is an individual or a company that provides Dermofix active pharmaceutical ingredient (API) or Dermofix finished formulations upon request. The Dermofix suppliers may include Dermofix 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 Dermofix Drug Master File in Korea (Dermofix KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Dermofix. The MFDS reviews the Dermofix KDMF as part of the drug registration process and uses the information provided in the Dermofix KDMF to evaluate the safety and efficacy of the drug.
After submitting a Dermofix 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 Dermofix API can apply through the Korea Drug Master File (KDMF).
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