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Daiichi Sankyo Europe GmbH

Division of Daiichi Sankyo Co. Ltd.
www.daiichi-sankyo.de

Latest From Daiichi Sankyo Europe GmbH

Orphan AML Products Face CHMP Questioning

Companies developing new AML treatments are among those being called before the European Medicines Agency this week for questioning over marketing applications approaching the end of the review process. 

Europe Drug Review

Novartis’s Zolgensma Loses EU Accelerated Assessment

Companies pleased at gaining an EU accelerated assessment for a product should be aware that the agency offers no guarantee that they will get to keep it. Novartis’s Zolgensma is one of seven drugs whose review the EMA has taken off the fast track.

Europe Drug Review

EU Accelerated Assessment – Hard To Get, Hard To Keep

It’s hard enough in the first place for companies to persuade the European Medicines Agency that their planned marketing authorization application should be fast-tracked. Many are also finding that after accelerated assessment is granted, it is taken away during the actual review.

Review Pathway Drug Review

New Filings At The EMA

New medicines under evaluation at the European Medicines Agency.

Drug Review Europe
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Company Information

  • Industry
  • Pharmaceuticals
  • Therapeutic Areas
  • Non-Specific
  • Alias(es)
  • Daiichi Sankyo Deutschland GMBH
  • Ownership
  • Private
  • Headquarters
  • Worldwide
    • Europe
      • Western Europe
        • Germany
  • Parent & Subsidiaries
  • Daiichi Sankyo Co. Ltd.
  • Senior Management
  • Jan Van Ruymbeke, CEO
  • Contact Info
  • Daiichi Sankyo Europe GmbH
    Zielstrattstr. 48
    Munich, 81379
    Germany
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