Bachem Group is a public, innovation-driven company specializing in the development and manufacturing of peptides and oligonucleotides.
01 1Bachem SA
02 1Fermion Oy, Hanko plant
03 3Divi's Laboratories Limited
04 1Shandong Xinhua Pharmaceutical Co.,Ltd
05 1Zhejiang Chiral Medicine Chemicals Co., Ltd@(주)국전약품
06 1Zhejiang Wild Wind Pharmaceutical Co., Ltd
Bachem Group is a public, innovation-driven company specializing in the development and manufacturing of peptides and oligonucleotides.
Registrant Name : Kukjeon Pharmaceutical Co., Ltd.
Registration Date : 2021-03-03
Registration Number : 20210303-211-J-655
Manufacturer Name : Bachem SA
Manufacturer Address : Succursale of Vionnaz, Route du Simplon 22, 1895 Vionnaz, Switzerland
With Fermion, start the journey of your innovative API.
Registrant Name : Alvogen Korea Co., Ltd.
Registration Date : 2022-01-10
Registration Number : 20220110-211-J-1205
Manufacturer Name : Fermion Oy, Hanko plant
Manufacturer Address : Orioninkatu 2, Hanko, FI-10900, Finland
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PharmaCompass offers a list of Carbidopa 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 Carbidopa manufacturer or Carbidopa supplier for your needs.
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A RYTARY manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of RYTARY, including repackagers and relabelers. The FDA regulates RYTARY manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. RYTARY 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 RYTARY supplier is an individual or a company that provides RYTARY active pharmaceutical ingredient (API) or RYTARY finished formulations upon request. The RYTARY suppliers may include RYTARY 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 RYTARY Drug Master File in Korea (RYTARY KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of RYTARY. The MFDS reviews the RYTARY KDMF as part of the drug registration process and uses the information provided in the RYTARY KDMF to evaluate the safety and efficacy of the drug.
After submitting a RYTARY 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 RYTARY API can apply through the Korea Drug Master File (KDMF).
click here to find a list of RYTARY suppliers with KDMF on PharmaCompass.
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