Site/Sponsor Relationships
Beginner’s Guide to eTMF, eISF, and Regulatory Research Documents
Global & FDA regulations dictate how researchers organize & store trial documents. Learn the basics of eTMF & eISF clinical research tools
Advarra Launches Cloud-Based Secure Document Exchange to Accelerate Study Startup
Solution provides end-to-end integration and automated, seamless exchange of research documents between sites, sponsors, and CROs
A Checklist for Optimizing Clinical Trial Study Startup Activities
This checklist outlines key milestones and considerations for sites and sponsors in the clinical trial study startup process.
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.
Improved Research Workflows Begin with Perspective
Explore cross-industry feedback from stakeholders to better investigate key research workflows.
5 Considerations for Evaluating an eIRB System
Provide guidance for research requests to the IRB, identify the appropriate regulations, and simplify the process from submission to review.
Research Site Perspectives on Sponsor-provided Technology
This report outlines key survey findings, and offers suggestions as we work towards an industry-wide solution
The Powerful Potential of Open Collaboration
Explore key takeaways from the Consortium’s first in-person meeting at the Onsemble Conference and welcome new members.
Reuniting and Reconnecting at the 2022 Onsemble Conference
The 2022 Onsemble Conference provided an opportunity for attendees to reconnect in person and collaborate to move research forward.
Improving Regulatory Workflows in Study Startup
This newsletter outlines the Consortium's efforts to improve regulatory workflows in study startups.
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.
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