EMA advises on gathering patient feedback for oncology medicines

Published: 12-May-2016
Regulatory

Advises on how patient-reported outcome data should be integrated in oncology clinical trials


The European Medicines Agency (EMA) has published new guidance on using patient-reported outcome (PRO) measures in oncology studies. It outlines principles of scientific best practice rather than prescribing particular approaches to selecting and using PROs and advises on how patient-reported outcome data should be integrated in oncology clinical trials.

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