Aspen API. More than just an API.
01 1Aspen notre dame de bondeville@Ajinomoto Omnichem@Aspen Oss BV@ORIL Industrie
01 1Handok Co., Ltd.
01 1Fondaparinux sodium
01 1Netherlands
Registrant Name : Handok Co., Ltd.
Registration Date : 2013-03-29
Registration Number : 20130329-193-I-126-01
Manufacturer Name : Aspen notre dame de bondevil...
Manufacturer Address : 1, rue de l'Abbaye, 76960 Notre Dame De Bondeville@Cooppallaan 91, Wetteren, Oost-Vla...
A Fondaparinux Sodium manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Fondaparinux Sodium, including repackagers and relabelers. The FDA regulates Fondaparinux Sodium manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Fondaparinux Sodium 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 Fondaparinux Sodium manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Fondaparinux Sodium supplier is an individual or a company that provides Fondaparinux Sodium active pharmaceutical ingredient (API) or Fondaparinux Sodium finished formulations upon request. The Fondaparinux Sodium suppliers may include Fondaparinux Sodium API manufacturers, exporters, distributors and traders.
click here to find a list of Fondaparinux Sodium 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 Fondaparinux Sodium Drug Master File in Korea (Fondaparinux Sodium KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Fondaparinux Sodium. The MFDS reviews the Fondaparinux Sodium KDMF as part of the drug registration process and uses the information provided in the Fondaparinux Sodium KDMF to evaluate the safety and efficacy of the drug.
After submitting a Fondaparinux Sodium 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 Fondaparinux Sodium API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Fondaparinux Sodium suppliers with KDMF on PharmaCompass.
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