01 1Alembic Pharmaceuticals Limited
01 1Bosutinib
01 1India
Registration Number : 306MF10032
Registrant's Address : Alembic Road, Vadodara 390 003, Gujarat, India
Initial Date of Registration : 2024-02-21
Latest Date of Registration : 2024-02-21
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PharmaCompass offers a list of Bosutinib 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 Bosutinib manufacturer or Bosutinib supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Bosutinib manufacturer or Bosutinib supplier.
PharmaCompass also assists you with knowing the Bosutinib API Price utilized in the formulation of products. Bosutinib API Price is not always fixed or binding as the Bosutinib Price is obtained through a variety of data sources. The Bosutinib Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A DB8 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of DB8, including repackagers and relabelers. The FDA regulates DB8 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. DB8 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 DB8 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A DB8 supplier is an individual or a company that provides DB8 active pharmaceutical ingredient (API) or DB8 finished formulations upon request. The DB8 suppliers may include DB8 API manufacturers, exporters, distributors and traders.
click here to find a list of DB8 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 DB8 Drug Master File in Japan (DB8 JDMF) empowers DB8 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 DB8 JDMF during the approval evaluation for pharmaceutical products. At the time of DB8 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 DB8 suppliers with JDMF on PharmaCompass.
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