Racial Diversity in Clinical Trials: Building Trust in Participant Engagement
Racial Diversity in Clinical Trials: Building Trust in Participant Engagement While racial and ethnic diversity in clinical trial participation has […]
The Critical Role Sites Play in the Evolution of Clinical Trials
Drawing on the perspectives of experts from Parexel and Advarra, this white paper explores the evolving role of technology in clinical research and its impact on research sites and study conduct.
Global CRO Drives Study Startup Efficiency by Converting Local IRB Sites to Central IRB Review
Discover how Advarra helped a global CRO streamline site management, cut activation times, and improve cost efficiency through central IRB review.
Clinical Research in the COVID-19 Era: Methods for Continuity
The COVID-19 pandemic has led to a significant shift in day-to-day research operations. To keep research moving forward, sponsors need to build a solid foundation to support the virtualization of key components of clinical trials. In addition, the industry needs to maintain a participant-centric approach while ensuring participant safety and regulatory compliance throughout the trial.
Large Hospital System Requires Central IRB Partner
Learn how a large hospital system partnered with Advarra to establish a central IRB, streamlining oversight, training, and investigator support.
Part 11/Annex 11 Independent Audit and Compliance Assessment
Independent verification of compliance opens new doors for CRIO, Inc. and provides customers confidence that they can incorporate the eSource system into their own computer software validation strategy.
Comparative Analysis for Non-IND Sites
Advarra Consulting provides in-depth analysis of German, European, and US regulations, allowing a cancer research study to move forward.
Informed Consent: 6 Approaches to Increase Participant Comprehension
Learn how applying health literacy principles, fostering discussions, and using teach-back methods can improve informed consent comprehension.
Managing Conflicts of Interest in Clinical Research
Explore key elements of managing conflicts of interest in clinical research, including COI policies, IRB roles, and regulatory agency guidance.
Botanical Medicines in Research
Learn how IRBs can approach botanical medicine protocols, addressing regulatory landscapes, ethical issues, and research safety.
Special Considerations for Pediatric Trials
Clinical research with minors poses several significantly different issues than research conducted on adults. Therefore, researchers must address a number of special considerations when conducting any pediatric clinical trial.
10 Tips for Writing Compliant Participant Materials
Learn how to craft compliant participant materials with tips on regulations, language to avoid, and effective phone screening scripts.