01 1Pharma Mar, S. A.
01 1Lurbinectedin
01 1Spain
Registration Number : 308MF10008
Registrant's Address : Avenida de los Reyes 1, P. I. La Mina 28770 Colmenar Viejo, Madrid, Spain
Initial Date of Registration : 2026-01-08
Latest Date of Registration : 2026-01-08
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PharmaCompass offers a list of Lurbinectedin 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 Lurbinectedin manufacturer or Lurbinectedin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Lurbinectedin manufacturer or Lurbinectedin supplier.
PharmaCompass also assists you with knowing the Lurbinectedin API Price utilized in the formulation of products. Lurbinectedin API Price is not always fixed or binding as the Lurbinectedin Price is obtained through a variety of data sources. The Lurbinectedin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Lurbinectedin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Lurbinectedin, including repackagers and relabelers. The FDA regulates Lurbinectedin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Lurbinectedin 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 Lurbinectedin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Lurbinectedin supplier is an individual or a company that provides Lurbinectedin active pharmaceutical ingredient (API) or Lurbinectedin finished formulations upon request. The Lurbinectedin suppliers may include Lurbinectedin API manufacturers, exporters, distributors and traders.
click here to find a list of Lurbinectedin 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 Lurbinectedin Drug Master File in Japan (Lurbinectedin JDMF) empowers Lurbinectedin 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 Lurbinectedin JDMF during the approval evaluation for pharmaceutical products. At the time of Lurbinectedin 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 Lurbinectedin suppliers with JDMF on PharmaCompass.
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