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PharmaCompass offers a list of Heparin 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 Heparin Sodium manufacturer or Heparin Sodium supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Heparin Sodium manufacturer or Heparin Sodium supplier.
PharmaCompass also assists you with knowing the Heparin Sodium API Price utilized in the formulation of products. Heparin Sodium API Price is not always fixed or binding as the Heparin Sodium Price is obtained through a variety of data sources. The Heparin Sodium Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Bemiparin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Bemiparin, including repackagers and relabelers. The FDA regulates Bemiparin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Bemiparin 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 Bemiparin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Bemiparin supplier is an individual or a company that provides Bemiparin active pharmaceutical ingredient (API) or Bemiparin finished formulations upon request. The Bemiparin suppliers may include Bemiparin API manufacturers, exporters, distributors and traders.
click here to find a list of Bemiparin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The Bemiparin Drug Master File in Japan (Bemiparin JDMF) empowers Bemiparin API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the Bemiparin JDMF during the approval evaluation for pharmaceutical products. At the time of Bemiparin JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of Bemiparin suppliers with JDMF on PharmaCompass.
We have 13 companies offering Bemiparin
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