Best of March: Top 5 Insights In Clinical Trial Technology

#1 - Pros & Cons Of Using Wearables In Clinical Trials

What are the biggest advantages and challenges of using wearables in a clinical trial? And who do you need on your team to add wearables to a trial? These are the questions Bryan Hansen, Ph.D. of Johnson & Johnson Innovative Medicine answers in this Q&A.

#2 - Overcoming Issues Of Non-Enrolling Sites In Clinical Trials

Explore the challenges of non-enrolling sites in clinical trials, focusing on the benefits of leveraging artificial intelligence (AI) and machine learning (ML) in addressing those issues. 

#3 - Why Is Trust Stifling Our RBM Implementations?

It’s one thing to implement RBM (risk-based monitoring) components like central monitoring or initial risk assessments, but if you’re still doing 100% SDR/SDV, you’re not maximizing the benefits of this approach. So what’s the holdup?

#4 - Using Virtual Study Coordinators For EDC Entry And Query Resolution To Speed Up Data Access And Cleaning

In this case study, learn about the integration of virtual study coordinators to optimize electronic data capture (EDC) processes in clinical research and how utilizing CRIO can enhance site performance, supporting recruitment and diversity objectives for sponsors.

#5 - Is Double Programming Really Required For Validation?

Double programming has been the gold standard for validation, but technological advancements and improved sponsor oversight of CRO deliverables have introduced more efficient and reliable alternatives.