Month: August 2026
Medical Imaging Is Strategic Data Historically, organizations often viewed imaging repositories as storage solutions. Today, imaging assets represent valuable clinical research data that support efficacy assessments, safety monitoring, and critical endpoint evaluation. Sponsors need more than storage; they need imaging workflow management. What Happens After Upload? Upload Verification De-identification Quality review Reader assignment Adjudication Archival…
Why Speed Matters Every day a study remains in startup mode represents lost opportunity. Sponsors face pressure to activate sites faster, begin enrollment sooner, reach milestones more quickly, and control operational costs. Technology implementation can significantly influence these timelines. Traditional EDC Challenges Many EDC implementations require extensive customization and lengthy configuration cycles. Common challenges include…
Modern Trials Depend on Imaging Data Medical imaging plays a critical role across numerous therapeutic areas, including oncology, neurology, cardiology, inflammatory diseases, and rare disease research. As imaging endpoints become more prevalent, organizations must manage increasing volumes of DICOM files, metadata, image reviews, adjudication workflows, and regulatory requirements. Many organizations still handle imaging separately from…
— FDA clearance of the IND, together with the previously cleared CTA, establishes a global Phase 1/2 clinical program for PM577a — — PM577a targets the H1069Q mutation in the ATP7B gene, the most prevalent WD-causing allele in North America and Europe — — Initial clinical data expected in 2027 — Excerpt from the Press…