Newsletter | July 15, 2026

07.15.26 -- STREAM Edition: Improve Patient Retention, Rapid Study Design, And Monitoring Quality

"We'll Figure It Out Later" Is Where Trial Friction Begins

Article | Scout

Delayed operational decisions around travel, payments, site workflows, meetings, and compliance can create avoidable friction for sites, participants, sponsors, and CROs once a study is underway.

How To Improve Patient ID And Retention In Chronic Disease Trials

Webinar | PPD Clinical Research Business of Thermo Fisher Scientific

Leveraging primary care for chronic disease studies can accelerate patient identification, access to underrepresented populations, and improve retention rates.

Rapid Study Design With The Sculptor Portal

Video | IQVIA Technologies

Accelerate your eCOA assessment design to streamline UAT, mid-study updates, and protocol amendments effortlessly.

Using Technology To Reduce Monitoring Costs And Increase Quality

Webinar | CRIO

Join industry experts as they discuss how the true value of DDC lies not just in the technology's cost, but in the operational efficiencies it unlocks.

Turning Messy Data Into Usable Evidence

Video | Clinical Tech Leader

Kathleen Mandziuk explains how transforming “messy” real-world data starts with clearly defining the research question, identifying available datasets, and addressing gaps. She highlights linking datasets, statistical methods, and balancing sample size with data limitations to generate meaningful evidence.

How AI Can Accelerate Clinical Trial And Registry Builds

Video | Crucial Data Solutions

AI tools speed study design — from protocol creation to validation and analysis — by automating complex tasks and generating intelligent data while preserving control, accuracy, and flexibility.

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