The Whole Product Approach
Learn how your organization can implement the Whole Product Approach and how Advarra uses this method to help research sites.
Improved Research Workflows Begin with Perspective
Explore cross-industry feedback from stakeholders to better investigate key research workflows.
A Holistic Approach to Ensuring Success with Your Technology Systems
In this webinar, we outline the Whole Product Approach, a comprehensive strategy focusing on all aspects of the user and site experience.
Clinical Trial Superheroes
Download this eBook to learn about the individuals who dedicate their talents to give patients an opportunity for healthier and longer lives.
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.
Advarra Releases Expanded Secure Document Exchange Capabilities as Part of Longboat Platform Release, Connecting Sites and Sponsors
Centralize the secure exchange of regulated documents between research stakeholders, streamlining study startup.
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.
Expedite Study Startup: Four Strategies to Optimize Site Activation
Learn how organizations can expedite study startup by streamlining site selection, training, ethics review, and site initiation.
Research Technology Staffing
Advarra has the unique product expertise and ability to fulfill multiple clinical research technology roles
The Impact of Digital Transformation in Clinical Trials
Explore what digital acceleration means for clinical research and how Advarra views digital transformation in the industry.
Improving Regulatory Workflows in Study Startup
This newsletter outlines the Consortium's efforts to improve regulatory workflows in study startups.