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 […]
For many clinical research staff members, recruiting participants for a study poses a challenge – sometimes a bigger challenge than […]
Discover how an NCI-designated hospital system trained 400 remote end users efficiently with Advarra’s Custom eLearning Solutions.
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.
This eBook outlines how to prepare for an upcoming FDA inspection, what to expect during the inspection, and steps to take following inspection close.
Learn how the Whole Product Approach helps research sites evaluate and implement technology tailored to their unique operational needs.
Download the case study to learn how Advarra’s Institutional Research CoE helped ensure compliance and maintained critical funding sources.
Discover how Advarra’s ICF writing services helped a site network create compliant, flexible processes, improving IRB submissions and timelines.
Navigating research compliance often means addressing unseen challenges. Explore strategies to identify blind spots and strengthen oversight frameworks.
Learn how DSMBs safeguard trial integrity and participant safety with insights on setup, member selection, and the importance of independence.
To better understand when you may need an endpoint adjudication committee (EAC), it’s helpful to know the EAC’s role in research.
Explore the contributions of clinical trial superheroes, from coordinators to data analysts, improving patient health and outcomes.
Discover how CDOs can balance productivity and quality by exploring agile approaches, benchmarking insights, and key elements of organizational redesign.