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 1Ozenoxacin
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 : 2021-12-10
Registration Number : Su403-3-ND
Manufacturer Name : Interquim, SA
Manufacturer Address : Joan Buscallà 10 E-08173 Sant Cugat del Vallès (Barcelona), Spain
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PharmaCompass offers a list of Ozenoxacin 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 Ozenoxacin manufacturer or Ozenoxacin supplier for your needs.
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A 245765-41-7 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 245765-41-7, including repackagers and relabelers. The FDA regulates 245765-41-7 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 245765-41-7 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 245765-41-7 supplier is an individual or a company that provides 245765-41-7 active pharmaceutical ingredient (API) or 245765-41-7 finished formulations upon request. The 245765-41-7 suppliers may include 245765-41-7 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 245765-41-7 Drug Master File in Korea (245765-41-7 KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of 245765-41-7. The MFDS reviews the 245765-41-7 KDMF as part of the drug registration process and uses the information provided in the 245765-41-7 KDMF to evaluate the safety and efficacy of the drug.
After submitting a 245765-41-7 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 245765-41-7 API can apply through the Korea Drug Master File (KDMF).
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