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Riley Farley

Accelerate Clinical Trial Cycle Times at Academic Medical Centers and Health Networks with eReg/eISF

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Accelerate Clinical Trial Cycle Times at Academic Medical Centers and Health Networks with eReg/eISF

The adoption of eReg/eISF solutions in clinical trials can significantly improve outcomes across Academic Medical Centers (AMCs) and health networks, where efficient regulatory documentation management is essential. eReg/eISF solutions, electronic platforms specifically designed for regulatory document and process management in clinical trials, streamline the entire workflow, from document creation and secure storage to real-time access … Read more

Innovative Patient Recruitment: A Site Spotlight on Cedar Health Research

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Innovative Patient Recruitment: A Site Spotlight on Cedar Health Research

The Irving Aging Well Expo in September 2024 drew over 2,000 attendees eager to learn about the latest in health and wellness, and Cedar Health Research (CHR) emerged as a standout participant. Leveraging a revamped patient recruitment strategy and the industry’s most comprehensive eClinical technology, CHR demonstrated how innovation and a fully integrated platform could … Read more

How eSource Improves Clinical Trials: 5 Key Benefits

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The shift from traditional paper-based methods to electronic source data (eSource) platforms is reshaping data collection and management in clinical trials. In its Draft Electronic Source Data in Clinical Investigations Guidance Document, the FDA has recognized the growing importance of electronic systems in improving data integrity and compliance in clinical investigations. While there is an … Read more

Leading Clinical Trials with Precision: Tracking Performance that Delivers Results

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Leading Clinical Trials with Precision

Why Tracking Performance Metrics Matters Academic Medical Centers (AMCs) and health networks, tasked with managing a diverse portfolio of clinical trials, face significant challenges in maintaining operational efficiency, data integrity, and regulatory compliance. One pivotal strategy to navigate this challenging environment is the effective capture and tracking of key performance metrics (KPIs). These clinical trial … Read more

eReg/eISF in Clinical Trials – 8 Trends Driving Adoption

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In our blog, “What is eRegulatory in Clinical Trials,” we explored four key trends fueling the adoption of eReg/eISF across Academic Medical Centers (AMCs), sites, site networks, and sponsors. In this follow-up, we dive deeper, expanding on four additional trends driving eReg/eISF in clinical trials.  The transition from paper-based systems or disconnected platforms to integrated … Read more

From Study Start-up to Execution: How to Centralize Visibility and Performance Transparency in Clinical Trials 

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Academic Medical Centers (AMCs), sites, and health networks are constantly striving to streamline processes, reduce timelines, and improve outcomes. Central to achieving these goals is the ability to manage trials effectively, ensuring all key players have the data they need to make informed decisions. If you are looking to view, manage, and optimize site performance from … Read more

eSource vs EHR/EMR: Why Sites Use eSource for Clinical Trials 

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eSource vs EHR/EMR: Why sites use eSource in clinical trials

The integration of technology in clinical trials increases accuracy, efficiency, and regulatory compliance. While both Electronic Health Records (EHRs) and electronic Source Data (eSource) systems are key components in this shift, they serve fundamentally different functions within the clinical trial process. What’s the difference? EHRs primarily focus on patient care and are intended for clinical workflows, whereas … Read more

RealTime eClinical Solutions Emerges as a Choice Vendor for Nine of the Top 10 Global Site Networks

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This press release was initially published on Cision/PR Newswire. You can view the original release here. SAN ANTONIO, Texas, (September 10, 2024) – RealTime eClinical Solutions, a leader in clinical trial technology, proudly announces its continued success as a choice vendor for leading site networks with the widespread adoption of its integrated eClinical product suite. … Read more

Reduce Timelines in Clinical Trials – How to Standardize Study Start-Up and Capture Timing Metrics

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An analysis published in the National Library of Science identified that key drivers for start-up delays in clinical trials include categories such as inefficient processes/pitfalls as well as contracts and budgets. Academic Medical Centers (AMCs) and health networks conducting clinical trials are constantly striving to streamline trial workflows, reduce cycle times, and deliver faster, more … Read more

What is eRegulatory in Clinical Trials?  

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eRegulatory, often abbreviated as eReg or eReg/eISF (electronic investigator site file), refers to the use of electronic systems to manage regulatory documentation and compliance processes in clinical trials. eReg is an eClinical solution that streamlines the management of critical clinical trial documents. This safeguards that these important documents are securely stored, tracked, and accessed. Today, … Read more