01 1Pharma Mar, S. A.
01 1Trabectedin
01 1Spain
Registration Number : 226MF10132
Registrant's Address : Avenida de los Reyes 1, P. I. La Mina 28770 Colmenar Viejo, Madrid, Spain
Initial Date of Registration : 2014-07-02
Latest Date of Registration : 2024-11-27
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PharmaCompass offers a list of Trabectedin 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 Trabectedin manufacturer or Trabectedin supplier for your needs.
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PharmaCompass also assists you with knowing the Trabectedin API Price utilized in the formulation of products. Trabectedin API Price is not always fixed or binding as the Trabectedin Price is obtained through a variety of data sources. The Trabectedin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Ecteinascidin 743 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ecteinascidin 743, including repackagers and relabelers. The FDA regulates Ecteinascidin 743 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ecteinascidin 743 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Ecteinascidin 743 supplier is an individual or a company that provides Ecteinascidin 743 active pharmaceutical ingredient (API) or Ecteinascidin 743 finished formulations upon request. The Ecteinascidin 743 suppliers may include Ecteinascidin 743 API manufacturers, exporters, distributors and traders.
click here to find a list of Ecteinascidin 743 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 Ecteinascidin 743 Drug Master File in Japan (Ecteinascidin 743 JDMF) empowers Ecteinascidin 743 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 Ecteinascidin 743 JDMF during the approval evaluation for pharmaceutical products. At the time of Ecteinascidin 743 JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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