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More-EUROPA

We are a consortium of 15 European institutes which work towards a more efficient use of real-world data in the development, registration and assessment of medicinal products in Europe.
We are a consortium of 15 European institutes which work towards a more efficient use of real-world data in the development, registration and assessment of medicinal products in Europe.
While randomized controlled trials (RCTs) remain the mainstay in drug development, approval, and reimbursement, the potential of real world data (RWD) to contribute to the understanding of drug effects is increasingly realized.
The aim of our project is to develop, implement and establish evidentiary standards and methods to address the data and evidentiary needs of regulatory authorities and health technology assessment (HTA) bodies towards a more efficient use of RWD for the development, registration and assessment of medicinal products in Europe.

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E-mail: [email protected]

Lysbeth Bakker, project manager
Peter Mol, project coordinator
Sieta de Vries, project co-lead

More-EUROPA is funded by the European Union.  Grant agreement number: 101095479. Views and opinions expressed are however those of the author(s) only and do not necessarily reflect those of the European Union or the European Commission. Neither the European Union nor the granting authority can be held responsible for them. 

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