Featured Articles
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How The New EU Clinical Trials Regulation Will Impact Sites And Sponsors And How You Can Prepare
4/25/2022
The Clinical Trials Regulation (CTR) for the EU took effect on 31 January 2022. Sites and sponsors must now embrace the new regulations to successfully run clinical trials across the European Union.
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Decentralization Of Clinical Trials Requires Digitization Of Clinical Trials – Is The Industry Wired For This Revolution?
3/21/2022
Learn how the end result to decentralized trials is greater patient-centricity, higher enrollment, fewer drop-outs, and a faster study timeline.
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Using Change Management For Digital Transformations In Clinical Trials
2/28/2022
Once you’ve implemented a new software or process into your clinical trial organization, you may find yourself asking, “Now what?” The answer to that is simple: focus on change management.
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7 Key Findings From A Clinical Trial Operations Technology Survey
1/19/2022
To stay competitive in the clinical research field, sites, sponsors, and CROs need to invest in remote technology. Discover seven key trends that your clinical trial team needs to know about.
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Helping Your Research Site Go Paperless
12/8/2021
In the available article, read about the three common concerns about going paperless with clinical research.
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How Remote Site Access Is Changing Clinical Operations
11/2/2021
How can always-on remote site access benefit your research organization? Read about these benefits and the importance of reliable, efficient remote site access.
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How To Advance Your Career With Digital Research Certifications
10/26/2021
In this article, read how the explosion in remote clinical trial technology over the past two years has changed how clinical research teams work together.
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How The Right Software Can Help Sites And Sponsors Navigate The FDA Approval Process
8/26/2021
Sponsors, CROs, and research sites in the U.S. have always understood the importance of the FDA approval process. But with the arrival of COVID-19 vaccines, the general public has started paying closer attention to the FDA’s actions.
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Remote Connectivity Is Now A Requirement In The Site, Sponsor, And CRO Relationship
8/26/2021
“Within hours, our clinical operations had to be fully remote. Patients couldn’t come on-site. Our team couldn’t get into the clinic. But we had to keep our studies on track and needed to continue to monitor patient safety,” says Catherine Gregor, Director of Clinical Research Administration for Vanderbilt-Ingram Cancer Center.
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Remote Site Access Solutions: 5 Questions to Include in your RFI
7/27/2021
Many sites in the current pandemic landscape have limited or restricted on-site monitoring visits, increasing the demand for remote site access solutions across the industry. Read how the accelerating digital transformation stems from sponsors and CROs needing access to essential regulatory documents and source data from their sites.