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How to Collect and Measure Diversity Data Early in Your Clinical Trials

Within the FDA’s guidance document issued in August 2023: Postmarketing Approaches to Obtain Data on Populations Underrepresented in Clinical Trials for Drugs and Biological ...
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9 Ways to Reduce Clinical Trial Site Burden

As leaders in clinical research, sponsors can have the ability to drastically reduce elements of clinical trial site burden.
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Increasing Diversity in Clinical Trials? Here’s How to Know if You’re on Track with Your Diversity Plan.

In 2022, the FDA provided draft guidance around diversity plans for sponsors to improve the enrollment of clinical trial participants from underrepresented racial and ethnic ...
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How to Increase Enrollment: 17 Ways Research Sites Can Improve Clinical Trial Workflows

We have seen clinical research sites accelerate their patient enrollment timeline by four weeks. We have also seen sites enroll 41% more patients in a clinical trial than industry ...
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5 Ways Sponsors Can Speed Up Enrollment for Rare Disease Clinical Trials

Only about 5% of rare diseases have at least one approved treatment available for affected patients. To increase the availability of care options in this therapeutic area, sponsors ...
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Why Pre-screening Data Matters in Clinical Trials That Are on Track with Enrollment

Even if your clinical trial enrollment is on track, it is still worthwhile to invest in making recruitment the smoothest–and fastest–it can be. Optimizing your approach with deeper ...
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