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
Aspen API. More than just an API™
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...
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PharmaCompass offers a list of Fondaparinux Sodium 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 Fondaparinux Sodium manufacturer or Fondaparinux Sodium supplier for your needs.
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PharmaCompass also assists you with knowing the Fondaparinux Sodium API Price utilized in the formulation of products. Fondaparinux Sodium API Price is not always fixed or binding as the Fondaparinux Sodium Price is obtained through a variety of data sources. The Fondaparinux Sodium Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Arixtra manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Arixtra, including repackagers and relabelers. The FDA regulates Arixtra manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Arixtra 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 Arixtra manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Arixtra supplier is an individual or a company that provides Arixtra active pharmaceutical ingredient (API) or Arixtra finished formulations upon request. The Arixtra suppliers may include Arixtra API manufacturers, exporters, distributors and traders.
click here to find a list of Arixtra 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 Arixtra Drug Master File in Korea (Arixtra KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Arixtra. The MFDS reviews the Arixtra KDMF as part of the drug registration process and uses the information provided in the Arixtra KDMF to evaluate the safety and efficacy of the drug.
After submitting a Arixtra 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 Arixtra API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Arixtra suppliers with KDMF on PharmaCompass.
