A Checklist for Optimizing Clinical Trial Study Startup Activities
From protocol design to site training, optimizing study startup requires meticulous planning and collaboration to ensure timely trial activation.
Technology
Best Practices in Pre-Screening Includes Use of Technology
Pre-screening subjects is common practice at most sites. In this article, learn some best practices and how technology can play an important role.
The ROI of eRegulatory and eIRB Integration
Integrating eRegulatory and eIRB systems streamlines document management, enhances compliance, and delivers significant ROI through time and cost savings per protocol.
The Whole Product Approach
Learn how the Whole Product Approach helps research sites evaluate and implement technology tailored to their unique operational needs.
Clinical Trial Superheroes
Explore the contributions of clinical trial superheroes, from coordinators to data analysts, improving patient health and outcomes.
Research Site Perspectives on Sponsor-provided Technology
Gain insights into site challenges with sponsor-provided technology, including system preferences, time metrics, and investigator platform experiences.
The Powerful Potential of Open Collaboration
Advarra’s Site-Sponsor Consortium emphasizes shared standards and transparent dialogue, paving the way for scalable, collaborative research advancements.
Reuniting and Reconnecting at the 2022 Onsemble Conference
Throughout the day on Tuesday, March 29, clinical research professionals arrived at the Westin Savannah Harbor Golf Resort & Spa
Expedite Study Startup: Four Strategies to Optimize Site Activation
Learn how organizations can expedite study startup and avoid delays through streamlining site selection, training, ethics review, and site initiation.
The Impact of Digital Transformation in Clinical Trials
Digital transformation. We’ve heard about it for years, but now all of us have experienced a dramatic technological acceleration as
