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.
Advarra Consulting provides in-depth analysis of German, European, and US regulations, allowing a cancer research study to move forward.
Learn how applying health literacy principles, fostering discussions, and using teach-back methods can improve informed consent comprehension.
Explore key elements of managing conflicts of interest in clinical research, including COI policies, IRB roles, and regulatory agency guidance.
Learn how IRBs can approach botanical medicine protocols, addressing regulatory landscapes, ethical issues, and research safety.
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.
Learn how to craft compliant participant materials with tips on regulations, language to avoid, and effective phone screening scripts.
Learn about the unique challenges of pediatric clinical trials, including federal regulations, minimal risk, and parental permissions.
Learn the essentials of expedited IRB review, including minimal risk criteria, eligible study procedures, and regulatory distinctions.
Discover how Advarra Insights helped UW Carbone Cancer Center reduce manual reporting and gain actionable visibility into accrual metrics and operations.
Discover the criteria for IRB review, including fully convened, designated member reviews, or exemption, with tips for better study planning.
Learn how UW Carbone Cancer Center leveraged Advarra EVAL to improve CCSG processes, saving resources while earning an “Outstanding” renewal grade.
Learn how IU’s Simon Cancer Center cut staff time by 52%, reduced inefficiencies, and optimized workflows with Advarra Participant Payments.