Articles, App Notes, Case Studies, & White Papers
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Unlocking New Clinical Insights With Remote Captured Sleep Data
3/25/2022
Physicians, researchers, and drug developers need better data on sleep but capturing rich, real-world data in formal clinical trials has been difficult. Gain insight into ways to start collecting quality sleep data remotely by leveraging cloud-based data ingestion and processing.
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Gradually Investing In Direct Data Capture Is Inevitable
2/2/2023
Given study decentralization and the many electronic sources of data now available, it is time for sponsors and contract research organizations to face the inevitable: EDCs need to be “sunsetted.”
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SMART On FHIR: Auto-Populate eCRFs On Study Day 1
7/10/2023
Get an overview of SMART on Fast Healthcare Interoperability (FHIR) for clinical trials, including workflow improvements, real-world data (RWD) integration, and reducing researcher burnout.
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The False Economy Of Paper Diaries In Clinical Trials
8/22/2022
While paper diaries may appear cheaper, but there are hidden costs that make a digital eCOA solution much more affordable in your clinical trial.
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Nevro Eliminates Majority Of Source Data Verification With ePRO And EDC
2/23/2023
Read how a global medical device company was able to unlock new efficiencies by implementing data collection via electronic patient-reported outcome assessments.
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Considerations For Implementing The Best eCOAs In Your Trial Design
5/2/2022
Dive into considerations when deciding on the best COAs to implement as well as best practices when developing your eCOA strategy in this blog.
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eTMF Systems Tell Compelling Story Of COVID-19 Vaccines
3/7/2022
The rapid development of Covid-19 vaccines may lead more drug developers to increase their speed and agility by adopting electronic Trial Master File (eTMF) systems. In the case of Covid-19 vaccines, discover how eTMF systems tell a dramatic tale.
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Managing Clinical Trial Changes And Mid-Study Data Migrations
11/15/2023
Explore how the Imperial College London was able to complete a successful migration of 14 ongoing studies, involving over 1,700 patients and 150,000+ forms, within a 16-month timeframe.
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Automation Solutions For Safety Document Distribution
5/27/2022
Discover how a leading global pharmaceutical company solved the problem of managed the distribution of safety reports by their clinical operations team.
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Simplifying The Regulatory Submission Process With A Modern CTMS
12/14/2022
Working in collaboration with industry representatives, explore the value that pulling the regulatory submission process into a modern Clinical Trial Management System (CTMS) could have.