08.25.26 -- AI Risk, Patient Ethics And eClinical Tools: What's Driving Trials Forward

A research compliance leader and a patient advocate explore how ethical oversight, privacy, and the IRB intersect while sharing a personal PMDD journey that shows the potential of participation.

Targeted prescreening for biomarker and cognitive criteria cut screen failures in a complex Alzheimer’s trial, speeding enrollment and improving site efficiency while maintaining strict eligibility.

Designing data capture around study protocols boosts data quality and real‑time visibility. Reducing transcription and aligning workflows helps teams improve compliance and speed decisions.

Comprehensive, validated laboratory testing paired with advanced instrumentation and seamless EDC integration helps streamline clinical trials without downtime or data gaps.

Simplify complex clinical trials with a unified eClinical orchestration solution that brings together core trial functions, including IRT, eCOA, visit and participant management, and supply oversight.

Automate protocol design, database builds, and validation to cut study setup from months to days — enabling faster analytics, earlier insights, and trial simulation.

Optimize flexible electronic patient-reported outcomes that allow participants to switch between site-owned devices, personal hardware, and remote completion.