The Future of Clinical Trials: Going Digital With Remote Monitoring
The COVID-19 pandemic changed the way that we people live and work. Everything went online, from ordering groceries to remote collaboration with coworkers. The vaccines
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Top Features in ETMF Software for Clinical Trials
With numerous eTMF software options available in the market, it is essential to know what features to look for when selecting the right solution for your clinical trials.
Finding the best CRO partner for your clinical trial
Learn how seasoned experts evaluate and successfully select CRO Partners
FDA Audit of eTMF Trial Master File System
SureClinical eTMF Passes FDA Inspection Clinical trial systems and processes are advancing at a fast rate. We’ve come a long way from truckloads of paper
SureClinical Launches Eclinical Ecosystem ECO Bundle to Support Clinical Trial Automation and Collaboration
Clinical operations ecosystem for Clinical Research Organizations streamlines and accelerates the delivery of new treatments to patients globally RENO, NV – December 16, 2021 –
Announcing the New SureClinical ECO Bundle for Clinical Operations
The challenges facing clinical trial teams today Life Science Clinical Operations teams struggle to connect, collect, access, view, report, analyze, and understand data from
What’s the difference between electronic signatures and digital signatures?
Every day, individuals are more and more likely to sign documents electronically. But, just what is an electronic signature? Are there different types of signatures?
Key “Critical to Quality” Factors in newly released ICH E8(R1) Guidance for Designing Quality into Your Clinical Trial
Clinical trials are incredibly important for bringing safe and effective treatments to market to help patients who need them. With that in mind, the International
Improving Clinical Trial ROI with Automation
Clinical trials continue to be burdened with paper and manual processes. Sometimes hybrid situations are used where there are some paper processes and some manual
The Importance of Sponsor Oversight in Clinical Trials
By Guest Author: Dr. Karin Köhler-Hansner As a sponsor, do you contract out your clinical trials to a CRO and forget about them? Do you