Therapeutic Innovation and Regulatory Science

The objective of this paper is to outline best practice recommendations for training end users, including site staff and study participants, on the use of ePRO technology in clinical trials to enable consistent, accurate, and complete data collection.

Published on behalf of the ePRO Consortium, this article recommends a structured framework for training site personnel and study participants in order to optimize the advantages clinical trial sponsors can gain from using ePRO data collection systems.

Read the full article here.

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