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Tips for Clinical Trial Sites: Hear from a Research Coordinator at Centre Hospitalier de Mont de Marsan

Meet research coordinator Anne-Helene Boivin of Centre Hospitalier de Mont de Marsan in France as she shares a quick look into the clinical trial workflow at her research site, ...
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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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How to Write Site-Friendly Protocol Amendments in Clinical Trials

Clinical trial protocol development and maintenance are some of the most critical steps in the lifecycle of a research study. One of the most common (and important) maintenance ...
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3 Ways Sponsors and Sites Can Improve Patient Slot Allocation in Early Phase Clinical Trials

Patient slot allocation can be a critical element of early phase clinical trials. There may be a limited number of spots in the trial for participants, and the process of enrolling ...
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4 Reasons Sites Need to Automate Processes Around Clinical Trial Billing

When you look at clinical trial site financials at a high level, gaps in invoice creation, gaps in billing, and gaps in payment reconciliation can all add up. That combination of ...
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