Farmak works in the development, production and marketing of APIs, Intermediates & Specialties// FDA inspected.
01 1Farmak, as
02 1EUROAPI FRANCE
03 1Sanofi Chimie
04 1Alivus Life Sciences Limited
05 1ScinoPharm Taiwan, Ltd.
Farmak works in the development, production and marketing of APIs, Intermediates & Specialties// FDA inspected.
Registrant Name : Gukjeon Co., Ltd.
Registration Date : 2013-12-19
Registration Number : Su4749-12-ND
Manufacturer Name : Farmak, as
Manufacturer Address : Na vlcinci 16/3, Klasterni Hradisko, 779 00 Olomouc, Czech Republic
EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
Registrant Name : Sanofi-Aventis Korea Co., Ltd.
Registration Date : 2012-08-31
Registration Number : 3025-5-ND
Manufacturer Name : EUROAPI FRANCE
Manufacturer Address : 4 La Paterie, 63480, Vertolaye, France
EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
Registrant Name : Sanofi-Aventis Korea Co., Ltd.
Registration Date : 2008-05-07
Registration Number : 3025-2-ND
Manufacturer Name : Sanofi Chimie
Manufacturer Address : Center de production de Vitry-sur-Seine9, Quai Jules Guesde 94403 Vitry SUR Seine Ced...
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PharmaCompass offers a list of Riluzole 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 Riluzole manufacturer or Riluzole supplier for your needs.
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A A13951 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of A13951, including repackagers and relabelers. The FDA regulates A13951 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. A13951 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 A13951 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A A13951 supplier is an individual or a company that provides A13951 active pharmaceutical ingredient (API) or A13951 finished formulations upon request. The A13951 suppliers may include A13951 API manufacturers, exporters, distributors and traders.
click here to find a list of A13951 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 A13951 Drug Master File in Korea (A13951 KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of A13951. The MFDS reviews the A13951 KDMF as part of the drug registration process and uses the information provided in the A13951 KDMF to evaluate the safety and efficacy of the drug.
After submitting a A13951 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 A13951 API can apply through the Korea Drug Master File (KDMF).
click here to find a list of A13951 suppliers with KDMF on PharmaCompass.
We have 4 companies offering A13951
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