Data Management
eClinical Regulatory Trends Impacting Clinical Research
Understand current regulatory trends in clinical research and how it will shape the industry moving forward.
Beginner’s Guide to Clinical Trial Management Systems
A clinical trial management system (CTMS) can bring powerful efficiencies, insights, and compliance to sites' day-to-day operations.
eSource Study Build Services
Advarra’s eSource Study Build Services delivers high quality study builds and forms in Advarra eSource utilizing best practices in data capture and form design
Driving Site Efficiency and Visibility Using a CTMS
As clinical trials grow more complex, this eBook reviews how a CTMS may help your organization address challenges as you conduct research.
Manual Data Migration
Download the info sheet to learn about Advarra’s manual data migration services for various technology platforms.
Considerations for Transitioning from Paper to eSource
Explore the benefits of switching from paper to eSource, tips for implementation, and how to maintain compliance.
Maintaining Data & Reporting Integrity with Mobile Health
Understand how to properly handle and evaluate incoming data gathered using mobile health (mHealth) apps and technologies.
Video: Introduction to Data Monitoring Committees
More studies now require oversight than ever. DMCs are required when a trusted independent third party is necessary to assess clinical trials
Leveraging Data to Lead and Manage the Research Mission
This blog discusses how to use clinical data at all levels to lead and drive the research enterprise and day-to-day operations
Navigating the Ethics of Remote Research Data Collection
In this article, Luke Gelinas develops a framework to identify and address key challenges for remote research data collection.
Beginner’s Guide to Compliant Electronic Source Data Capture
Learn about electronic source data capture in clinical trials, relevant regulations, and best practices.
Enabling Compliant Remote Data Capture and Document Management
Download this white paper to learn how to establish consistent electronic processes to help manage clinical trials remotely.
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