EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
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01 1EUROAPI Germany GmbH
02 1EUROAPI Germany GmbH@Sanofi India Limited
03 1EUROAPI Germany GmbH@Sanofi-Aventis Deutschland GmbH
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01 3Handok Co., Ltd.
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01 3Ramifril
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01 3France
Registrant Name : Handok Co., Ltd.
Registration Date : 2024-02-06
Registration Number : 20240206-209-J-1365
Manufacturer Name : EUROAPI Germany GmbH@Sanofi ...
Manufacturer Address : Brueningstrasse 50, D711, D712, D721, D725, D731, D743, E610, E614, 65926, Frankfurt ...
Registrant Name : Handok Co., Ltd.
Registration Date : 2021-05-11
Registration Number : 20210511-209-J-983
Manufacturer Name : EUROAPI Germany GmbH@Sanofi-...
Manufacturer Address : Brueningstrasse 50, D711, D712, D721, D725, D731, D743, E610, E614, 65926, Frankfurt ...
Registrant Name : Handok Co., Ltd.
Registration Date : 2021-04-27
Registration Number : 20210427-209-J-953
Manufacturer Name : EUROAPI Germany GmbH
Manufacturer Address : Brueningstrasse 50, D711, D712, D721, D725, D731, D743, E610, E614, 65926, Frankfurt ...
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PharmaCompass offers a list of Ramipril 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 Ramipril manufacturer or Ramipril supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Ramipril manufacturer or Ramipril supplier.
PharmaCompass also assists you with knowing the Ramipril API Price utilized in the formulation of products. Ramipril API Price is not always fixed or binding as the Ramipril Price is obtained through a variety of data sources. The Ramipril Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Acovil manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Acovil, including repackagers and relabelers. The FDA regulates Acovil manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Acovil 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 Acovil manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Acovil supplier is an individual or a company that provides Acovil active pharmaceutical ingredient (API) or Acovil finished formulations upon request. The Acovil suppliers may include Acovil API manufacturers, exporters, distributors and traders.
click here to find a list of Acovil 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 Acovil Drug Master File in Korea (Acovil KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Acovil. The MFDS reviews the Acovil KDMF as part of the drug registration process and uses the information provided in the Acovil KDMF to evaluate the safety and efficacy of the drug.
After submitting a Acovil 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 Acovil API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Acovil suppliers with KDMF on PharmaCompass.