01 1Zhejiang Hisun Pharmaceutical. Co., Ltd.
01 1Korea United Pharmaceutical Co., Ltd.
01 1Dactinomycin
01 1China
Registrant Name : Korea United Pharmaceutical Co., Ltd.
Registration Date : 2020-07-14
Registration Number : 20200714-210-J-490
Manufacturer Name : Zhejiang Hisun Pharmaceutica...
Manufacturer Address : No. 56 Binhai Road, Jiaojiang District, Taizhou City, Zhejiang China
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PharmaCompass offers a list of Dactinomycin 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 Dactinomycin manufacturer or Dactinomycin supplier for your needs.
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A Dactinomicina manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Dactinomicina, including repackagers and relabelers. The FDA regulates Dactinomicina manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Dactinomicina 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 Dactinomicina manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Dactinomicina supplier is an individual or a company that provides Dactinomicina active pharmaceutical ingredient (API) or Dactinomicina finished formulations upon request. The Dactinomicina suppliers may include Dactinomicina API manufacturers, exporters, distributors and traders.
click here to find a list of Dactinomicina 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 Dactinomicina Drug Master File in Korea (Dactinomicina KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Dactinomicina. The MFDS reviews the Dactinomicina KDMF as part of the drug registration process and uses the information provided in the Dactinomicina KDMF to evaluate the safety and efficacy of the drug.
After submitting a Dactinomicina 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 Dactinomicina API can apply through the Korea Drug Master File (KDMF).
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