This column highlights how incorporating data from patient disease registries in a real-world data mix offers four impactful benefits for clinical researchers.
Dispatches collected from sources in the world beyond ACRP (no endorsements implied) and edited for your reading pleasure on diversity, equity, and inclusion in healthcare and research.
Clinical research professional respondents to a new survey reported overwhelmingly that having a mentor had a positive impact on their clinical research experience.
The clinical research “workforce must be diverse, with sites located in areas where underserved populations live.”
Now is the time to reflect on and apply what we’ve learned during the pandemic to make clinical trials better today and tomorrow.