Bachem Group is a public, innovation-driven company specializing in the development and manufacturing of peptides and oligonucleotides.
01 1Bachem SA, Succursale de Vionnaz
02 1EGIS PHARMACEUTICALS PUBLIC LIMITED COMPANY
03 1DIVI'S LABORATORIES LIMITED
04 1Daito Co., Ltd.
05 1Daiwa Pharmaceutical Industries Co., Ltd.
06 1Shandong Xinhua Pharmaceutical Co. , Ltd.
07 1Sicor Societa (') Italiana Corticosteroidi S. r. l.
08 1Zhejiang Wild Wind Pharmaceutical Co. , Ltd.
Bachem Group is a public, innovation-driven company specializing in the development and manufacturing of peptides and oligonucleotides.
Registration Number : 222MF10146
Registrant's Address : Route du simplon 22, CH-1895 Vionnaz-Switzerland
Initial Date of Registration : 2010-04-22
Latest Date of Registration : 2019-09-17
Egis is a Hungarian generic pharma company with 110 years history. Our activities incorporate all areas of the pharma value chain.
Registration Number : 220MF10226
Registrant's Address : H-1106 BUDAPEST KERESZTURI UT 30-38 HUNGARY
Initial Date of Registration : 2008-11-10
Latest Date of Registration : 2008-11-10
A Carbidopa manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Carbidopa, including repackagers and relabelers. The FDA regulates Carbidopa manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Carbidopa 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 Carbidopa manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Carbidopa supplier is an individual or a company that provides Carbidopa active pharmaceutical ingredient (API) or Carbidopa finished formulations upon request. The Carbidopa suppliers may include Carbidopa API manufacturers, exporters, distributors and traders.
click here to find a list of Carbidopa suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The Carbidopa Drug Master File in Japan (Carbidopa JDMF) empowers Carbidopa API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the Carbidopa JDMF during the approval evaluation for pharmaceutical products. At the time of Carbidopa JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of Carbidopa suppliers with JDMF on PharmaCompass.
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