Cohance Lifesciences, offers full range of CDMO services for small molecule APIs, intermediates, ADCs, Pellets and Formulations.
01 1Cohance Lifesciences Limited
02 1Juzen Chemical Corporation
01 1Dong-A ST Co., Ltd.
02 1M-Peak Korea Co., Ltd.
01 2Johnny Samid
01 1India
02 1Japan
Cohance Lifesciences, offers full range of CDMO services for small molecule APIs, intermediates, ADCs, Pellets and Formulations.
Registrant Name : M-Peak Korea Co., Ltd.
Registration Date : 2020-12-08
Registration Number : 20201208-211-J-593
Manufacturer Name : Cohance Lifesciences Limited
Manufacturer Address : API Unit-Ⅲ, Plot No. 3102/B, GIDC, Ankleshwar-393 002, Dist. Bharuch, Gujarat state...
Registrant Name : Dong-A ST Co., Ltd.
Registration Date : 2020-07-21
Registration Number : 20200721-211-J-423
Manufacturer Name : Juzen Chemical Corporation
Manufacturer Address : 1-10, Kiba-machi, Toyama-city, Toyama, 930-0806, Japan
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PharmaCompass offers a list of Zonisamide 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 Zonisamide manufacturer or Zonisamide supplier for your needs.
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A Excegran manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Excegran, including repackagers and relabelers. The FDA regulates Excegran manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Excegran 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 Excegran supplier is an individual or a company that provides Excegran active pharmaceutical ingredient (API) or Excegran finished formulations upon request. The Excegran suppliers may include Excegran 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 Excegran Drug Master File in Korea (Excegran KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Excegran. The MFDS reviews the Excegran KDMF as part of the drug registration process and uses the information provided in the Excegran KDMF to evaluate the safety and efficacy of the drug.
After submitting a Excegran 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 Excegran API can apply through the Korea Drug Master File (KDMF).
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