Newsletter | May 15, 2025

05.15.25 -- Pros & Cons Of Using Wearables In Clinical Trials

FEATURED EDITORIAL

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.

INDUSTRY INSIGHTS

'Real' Evidence Generating Real Pre- And Post-Market Benefits

Review the current and future applications of RWD/E in drug discovery, clinical research, regulatory review and approval, and its role in promoting health equity and patient and provider access.

EHR Integration: Driving Clinical Trial Efficiency

Explore how clinical trials are integrating Electronic Health Records (EHRs) into trial workflows to better face the increasing demands for efficiency, cost reduction, and improved participant experiences.

Frequently Asked Questions About IRMS MAX

Improve your information access and capabilities with the definitive gold standard of medical information systems.

The FDA's Remote Regulatory Assessments: The Future Of Inspections

Remote Regulatory Assessments (RRAs) provide distinct advantages over traditional inspections, such as increased efficiency, reduced travel costs, and enhanced global oversight capabilities.

6 Key Ways Real-World Data Is Advancing Colorectal Cancer Therapies

Real-world data (RWD) is transforming Colorectal cancer (CRC) research by complementing traditional clinical trials, accelerating drug development, and improving patient outcomes.

The Promise Of IQVIA One Home For Sites: A Site CEO's Perspective

By providing research sites with a unified, streamlined interface, we can reduce operational friction, enhance collaboration, and ultimately accelerate the development of new therapies.