Newsletter | June 19, 2025

06.19.25 -- Is Double Programming Really Required For Validation?

FEATURED EDITORIAL

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.

INDUSTRY INSIGHTS

Top HEOR Trends

Real-world evidence (RWE) offers insights into the effectiveness of medical treatments in everyday settings, with various stakeholders utilize RWE to enhance healthcare.

Clinical Trials In The Age Of Cost Caps

On February 7, 2025, the NIH introduced a pivotal policy (NOT-OD-25-068), capping indirect cost recovery at 15% for research grants.

Parkinson's Disease: Leveraging Wearable DHTs

Wearable DHTs offer a solution to the challenges of measuring Parkinson's disease in clinical trials. Discover how these technologies can improve outcome measures and accelerate drug development.

eCOA Evolution: Have We Overcomplicated It?

eCOA has evolved from simple data collection to complex patient engagement platforms, raising concerns about added complexity. Explore innovative tools aimed at simplifying this complexity.

Breaking Through Barriers With Integrated Trial Optimization

In today’s complex clinical trial environment, optimizing trial design requires a multidimensional strategy that balances scientific rigor with real-world constraints.

How eConsent Improves The Trial Experience For Patients And Sites

In part one of this series, the author dives into how electronic consent platforms are simplifying and improving the trial experience for patients and sites.

What Is Electronic Data Capture And How Does It Simplify Data Management?

As EDC systems continue to evolve, they streamline workflows, enhance data security, and improve patient outcomes.

6 Ways Lab Data Can Improve Clinical Trials

Explore six key ways laboratory data strengthens the clinical trial process, focusing on how RWD enhances patient recruitment, accelerates screening workflows, and improves overall study outcomes.