01 1Jin Biopharm Co., Ltd.
01 1Jin Biopharm Co., Ltd.
01 1Chamomile Tincture
01 1South Korea
Registrant Name : Jin Biopharm Co., Ltd.
Registration Date : 2024-10-07
Registration Number : 20241007-211-J-1700
Manufacturer Name : Jin Biopharm Co., Ltd.
Manufacturer Address : 34, Dreamsandan 5-ro, Cheongbuk-eup, Pyeongtaek-si, Gyeonggi-do
97
PharmaCompass offers a list of Apigenin 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 Apigenin manufacturer or Apigenin supplier for your needs.
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A Chamomile manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Chamomile, including repackagers and relabelers. The FDA regulates Chamomile manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Chamomile 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 Chamomile manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Chamomile supplier is an individual or a company that provides Chamomile active pharmaceutical ingredient (API) or Chamomile finished formulations upon request. The Chamomile suppliers may include Chamomile API manufacturers, exporters, distributors and traders.
click here to find a list of Chamomile 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 Chamomile Drug Master File in Korea (Chamomile KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Chamomile. The MFDS reviews the Chamomile KDMF as part of the drug registration process and uses the information provided in the Chamomile KDMF to evaluate the safety and efficacy of the drug.
After submitting a Chamomile 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 Chamomile API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Chamomile suppliers with KDMF on PharmaCompass.
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