Innovative Patient Recruitment: A Site Spotlight on Cedar Health Research
October 23, 2024
The Irving Aging Well Expo in September 2024 drew over 2,000 attendees eager to learn about the latest in health
How eSource Improves Clinical Trials: 5 Key Benefits
October 22, 2024
The shift from traditional paper-based methods to electronic source data (eSource) platforms is reshaping data collection and management in clinical
Leading Clinical Trials with Precision: Tracking Performance that Delivers Results
October 17, 2024
Why Tracking Performance Metrics Matters Academic Medical Centers (AMCs) and health networks, tasked with managing a diverse portfolio of clinical
eReg/eISF in Clinical Trials – 8 Trends Driving Adoption
October 14, 2024
In our blog, “What is eRegulatory in Clinical Trials,” we explored four key trends fueling the adoption of eReg/eISF across
From Study Start-up to Execution: How to Centralize Visibility and Performance Transparency in Clinical Trials
September 30, 2024
Academic Medical Centers (AMCs), sites, and health networks are constantly striving to streamline processes, reduce timelines, and improve outcomes. Central
eSource vs EHR/EMR: Why Sites Use eSource for Clinical Trials
September 11, 2024
The integration of technology in clinical trials increases accuracy, efficiency, and regulatory compliance. While both Electronic Health Records (EHRs) and
Reduce Timelines in Clinical Trials – How to Standardize Study Start-Up and Capture Timing Metrics
September 5, 2024
An analysis published in the National Library of Science identified that key drivers for start-up delays in clinical trials include
What is eRegulatory in Clinical Trials?
September 3, 2024
eRegulatory, often abbreviated as eReg or eReg/eISF (electronic investigator site file), refers to the use of electronic systems to manage
