01 1Biocon Limited
01 1Everolimus (0.2% BHT)
01 1India
Registration Number : 307MF10060
Registrant's Address : 20th KM Hosur Road, Electronics City, Bengaluru-560 100, Karnataka, India.
Initial Date of Registration : 2025-05-14
Latest Date of Registration : 2025-05-14
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PharmaCompass offers a list of Everolimus 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 Everolimus manufacturer or Everolimus supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Everolimus manufacturer or Everolimus supplier.
PharmaCompass also assists you with knowing the Everolimus API Price utilized in the formulation of products. Everolimus API Price is not always fixed or binding as the Everolimus Price is obtained through a variety of data sources. The Everolimus Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Afinitor manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Afinitor, including repackagers and relabelers. The FDA regulates Afinitor manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Afinitor 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 Afinitor manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Afinitor supplier is an individual or a company that provides Afinitor active pharmaceutical ingredient (API) or Afinitor finished formulations upon request. The Afinitor suppliers may include Afinitor API manufacturers, exporters, distributors and traders.
click here to find a list of Afinitor 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 Afinitor Drug Master File in Japan (Afinitor JDMF) empowers Afinitor 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 Afinitor JDMF during the approval evaluation for pharmaceutical products. At the time of Afinitor 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 Afinitor suppliers with JDMF on PharmaCompass.
