01 1Zhejiang Huahai Pharmaceutical Co., Ltd.
01 1Sam-O Pharmaceutical Co., Ltd.
01 1Azelaic acid
01 1China
Registrant Name : Sam-O Pharmaceutical Co., Ltd.
Registration Date : 2025-08-26
Registration Number : 20250826-211-J-1987
Manufacturer Name : Zhejiang Huahai Pharmaceutic...
Manufacturer Address : Xunqiao, Linhai, Zhejiang 317024, China
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PharmaCompass offers a list of Azelaic Acid API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Azelaic Acid manufacturer or Azelaic Acid supplier for your needs.
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A Finevin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Finevin, including repackagers and relabelers. The FDA regulates Finevin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Finevin 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 Finevin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Finevin supplier is an individual or a company that provides Finevin active pharmaceutical ingredient (API) or Finevin finished formulations upon request. The Finevin suppliers may include Finevin API manufacturers, exporters, distributors and traders.
click here to find a list of Finevin suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA 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 Finevin Drug Master File in Korea (Finevin KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Finevin. The MFDS reviews the Finevin KDMF as part of the drug registration process and uses the information provided in the Finevin KDMF to evaluate the safety and efficacy of the drug.
After submitting a Finevin 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 Finevin API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Finevin suppliers with KDMF on PharmaCompass.
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