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PharmaCompass offers a list of Abacavir Sulfate 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 Abacavir Sulfate manufacturer or Abacavir Sulfate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Abacavir Sulfate manufacturer or Abacavir Sulfate supplier.
PharmaCompass also assists you with knowing the Abacavir Sulfate API Price utilized in the formulation of products. Abacavir Sulfate API Price is not always fixed or binding as the Abacavir Sulfate Price is obtained through a variety of data sources. The Abacavir Sulfate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Abacavir Sulphate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Abacavir Sulphate, including repackagers and relabelers. The FDA regulates Abacavir Sulphate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Abacavir Sulphate 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 Abacavir Sulphate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Abacavir Sulphate supplier is an individual or a company that provides Abacavir Sulphate active pharmaceutical ingredient (API) or Abacavir Sulphate finished formulations upon request. The Abacavir Sulphate suppliers may include Abacavir Sulphate API manufacturers, exporters, distributors and traders.
click here to find a list of Abacavir Sulphate 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 Abacavir Sulphate Drug Master File in Japan (Abacavir Sulphate JDMF) empowers Abacavir Sulphate 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 Abacavir Sulphate JDMF during the approval evaluation for pharmaceutical products. At the time of Abacavir Sulphate 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 Abacavir Sulphate suppliers with JDMF on PharmaCompass.
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