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 ...
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, ...
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, ...
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 ...
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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