EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
01 1EUROAPI Germany GmbH
02 1EUROAPI Germany GmbH@Sanofi India Limited
03 1EUROAPI Germany GmbH@Sanofi-Aventis Deutschland GmbH
01 3Handok Co., Ltd.
01 3Ramifril
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 ...
A Ramipril manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ramipril, including repackagers and relabelers. The FDA regulates Ramipril manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ramipril 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 Ramipril manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Ramipril supplier is an individual or a company that provides Ramipril active pharmaceutical ingredient (API) or Ramipril finished formulations upon request. The Ramipril suppliers may include Ramipril API manufacturers, exporters, distributors and traders.
click here to find a list of Ramipril 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 Ramipril Drug Master File in Korea (Ramipril KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Ramipril. The MFDS reviews the Ramipril KDMF as part of the drug registration process and uses the information provided in the Ramipril KDMF to evaluate the safety and efficacy of the drug.
After submitting a Ramipril 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 Ramipril API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Ramipril suppliers with KDMF on PharmaCompass.
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