Newsletter | January 9, 2025

01.09.25 -- What's The Deal With eConsent?

SPONSOR

Is it time to turn the page on your trial management practices? Join us Feb. 11-13 for Clinical Leader Solutions Expo: Tech Week as experts across EDC, IRT, and eCOA introduce the latest in technologies. We’ll help you discover whether it’s time to write your next chapter and connect you with the partners ready to help you do so – all from the convenience of your computer. Register today and finish your clinical trials story strong.

FEATURED EDITORIAL

What's The Deal With eConsent?

By Dan Schell, chief editor, Clinical Leader

Are you for or against eConsent? It’s odd that this technology has kind of become a polarizing topic in the clinical trials industry. To find out why, I decided to get some feedback from folks who have actually used it. 

INDUSTRY INSIGHTS

Site And Sponsor Harmonization For Speedy Startups, Monitoring

Article | Cognizant

Now more than ever, stakeholders need harmony among their disparate systems — and that starts with the right organizational mindset: a culture of connectivity. Here’s what our experts recommend.

How To Differentiate With A Unified eClinical Solution

Article | Signant Health

Clinical trials are increasingly complex for sites, sponsors, and CROs. In a recent webinar, experts shared how a unified eClinical platform simplifies operations and enhances data quality.

Study Start-Up Challenges: Hard Realities, Effective Strategies

White Paper | IQVIA Technologies

Launching a study is complex, and the time between protocol approval and the first patient visit has increased dramatically. How can companies reverse this trend and accelerate study start-ups?

Applying RWD: Use Cases And FDA Guidance

Webinar | Flatiron Health

This presentation delves into pragmatic approaches for clinical evidence generation and regulatory acceptance. It examines recent FDA draft guidance on integrating RWD/RWE in medical device studies.