01 1Korea Biochem Pharmaceutical Co., Ltd.
01 1Korea Biochem Pharmaceutical Co., Ltd.
01 1Indigo Carmine
01 1South Korea
Registrant Name : Korea Biochem Pharmaceutical Co., Ltd.
Registration Date : 2021-10-29
Registration Number : 20211029-211-J-1133
Manufacturer Name : Korea Biochem Pharmaceutical...
Manufacturer Address : 204 Sandan-gil, Jeonui-myeon, Sejong Special Self-Governing City
40
PharmaCompass offers a list of Indigo Carmine 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 Indigo Carmine manufacturer or Indigo Carmine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Indigo Carmine manufacturer or Indigo Carmine supplier.
A indigo manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of indigo, including repackagers and relabelers. The FDA regulates indigo manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. indigo 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 indigo manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A indigo supplier is an individual or a company that provides indigo active pharmaceutical ingredient (API) or indigo finished formulations upon request. The indigo suppliers may include indigo API manufacturers, exporters, distributors and traders.
click here to find a list of indigo 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 indigo Drug Master File in Korea (indigo KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of indigo. The MFDS reviews the indigo KDMF as part of the drug registration process and uses the information provided in the indigo KDMF to evaluate the safety and efficacy of the drug.
After submitting a indigo 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 indigo API can apply through the Korea Drug Master File (KDMF).
click here to find a list of indigo suppliers with KDMF on PharmaCompass.
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