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3 Benefits of eSource for the Principal Investigator in a Clinical Trial

According to a pharma FDA auditor, the biggest issue for compliance in clinical trials is oversight by principal investigators – or the lack thereof. As the principal investigator ...
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The Difference Between Screening and Enrollment in Clinical Trials

Clinical trial screening is one piece of the overall patient enrollment period. The screening phase immediately follows the recruitment period, during which a potential candidate ...
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Challenges and Solutions for Clinical Trial Sites: Hear From a Doctor at Esbjerg Hospital in Denmark

PhD student and medical doctor Dr. Elise Jonasson Nielsen works at the department of hepatology and gastroenterology at the Esbjerg Hospital, University Hospital of Southern ...
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How to Analyze Eligibility Criteria Early to Improve Diversity in Clinical Trials

When you ensure your clinical trials are set up to enroll a representative patient population, you’re more likely to keep timelines and goals on track across your portfolio. ...
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4 Ways StudyTeam’s eSource Solution Streamlines Site Workflows in Clinical Trials

The FDA’s 2013 guidance for electronic source data capture promotes the use of eSource in clinical trials to streamline investigations while improving the reliability, quality, ...
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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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