The Revolving Door of Research: The Resourceful Way to Run Trials
Learn how flexibility, location, and virtual tech are redefining research work in this eBook on the “revolving door” of industry resources.
Developing an Enterprise Roadmap to Post Authorization Safety Studies
Discover how a top 10 biopharma company partnered with Advarra Consulting to implement and manage compliant post-authorization safety studies (PASS).
Top Barriers to Participation in Clinical Trials
Recruiting study participants is one of the most challenging tasks in the clinical trial process, and arguably one of the
Patient Recruitment and Enrollment in Clinical Trials
For many clinical research staff members, recruiting participants for a study poses a challenge – sometimes a bigger challenge than
Large NCI-designated Hospital System Trains 400 End Users, Resulting in Increased Levels of Efficiency and Consistency
Discover how an NCI-designated hospital system trained 400 remote end users efficiently with Advarra’s Custom eLearning Solutions.
Advarra Consulting Delivers Clinical Trial Management Oversight
In this case study, learn how Advarra Consulting, Provided comprehensive clinical quality services, Enabled compliance with good clinical practice requirements, and Assessed and mitigated study startup risks.
Complete Guide to FDA Inspection Readiness
This eBook outlines how to prepare for an upcoming FDA inspection, what to expect during the inspection, and steps to take following inspection close.
The Whole Product Approach
Learn how the Whole Product Approach helps research sites evaluate and implement technology tailored to their unique operational needs.
Large Research Healthcare System Maintains Compliance through Internal Program Assessment
Download the case study to learn how Advarra’s Institutional Research CoE helped ensure compliance and maintained critical funding sources.
Large Clinical Research Site Network Streamlines Study Startup with Reliable, Timely ICF Writing Services
Discover how Advarra’s ICF writing services helped a site network create compliant, flexible processes, improving IRB submissions and timelines.
The IND Journey Phase I – Navigating Success
Navigating research compliance often means addressing unseen challenges. Explore strategies to identify blind spots and strengthen oversight frameworks.
Establishing and Operating a DSMB: Tips for Clinical Trial Success
Learn how DSMBs safeguard trial integrity and participant safety with insights on setup, member selection, and the importance of independence.