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 CI 912 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of CI 912, including repackagers and relabelers. The FDA regulates CI 912 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. CI 912 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 CI 912 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A CI 912 supplier is an individual or a company that provides CI 912 active pharmaceutical ingredient (API) or CI 912 finished formulations upon request. The CI 912 suppliers may include CI 912 API manufacturers, exporters, distributors and traders.
click here to find a list of CI 912 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price 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 CI 912 Drug Master File in Korea (CI 912 KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of CI 912. The MFDS reviews the CI 912 KDMF as part of the drug registration process and uses the information provided in the CI 912 KDMF to evaluate the safety and efficacy of the drug.
After submitting a CI 912 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 CI 912 API can apply through the Korea Drug Master File (KDMF).
click here to find a list of CI 912 suppliers with KDMF on PharmaCompass.
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