Ereg
The Regulatory Binder Checklist For Clinical Trial Sites
This checklist offers a comprehensive framework for managing all necessary essential regulatory documents efficiently.
Advantages and Considerations for an eRegulatory Implementation
Gain an understanding of what an eReg system is and the features available to streamline clinical trial regulatory management.
University of Nebraska Medical Center Streamlines Regulatory Management and Accelerates Study Startup with Advarra eReg
Learn how Advarra eReg helps UNMC support remote monitoring and how eReg helped address prevalent challenges in clinical research.
eReg Benefits for Clinical Research: Use Cases for all Types of Sites
Using an eRegulatory system can benefit any site, helping to increase productivity, improve compliance, and save money.
Bridging the Gap: A Standardized Approach to Clinical Trial Document Management
Representatives from the Advarra Site-Sponsor Consortium will discuss a standards-based integration and automation of research technology.
The ROI of eRegulatory and eIRB Integration
Learn about the benefits to integrating with technology systems such as email, eIRB, CTMS, and other eReg platforms as you increase ROI.
Addressing Research Technology Challenges to Gain Sponsor Buy-in
Encouraging site-owned technology platforms enables site staff to produce their best work, increasing the likelihood of a study’s success.
eClinical Regulatory Trends Impacting Clinical Research
Understand current regulatory trends in clinical research and how it will shape the industry moving forward.
Duke University Prioritizes Advarra eReg’s Site Centric Workflows within a Connected Research Ecosystem
Download the case study to learn more about how Advarra eReg’s site centric workflows streamlined Duke University’s clinical operations.
Ensuring a Successful and Collaborative SDLC Process
Find out how Advarra's approach to the SDLC lifecycle leads to successful collaborations among sites and sponsors.
How to Be Research Ready: Today and Beyond
If presented with a new study, are you prepared to take it on? Efficient study activation can set the pace for a successful clinical trial.
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