VSI's IRM Portal modernizes sponsor-investigator engagement in life-sciences trials by providing a single, secure digital platform for protocol distribution, site activation, and investigator communications. Key features include: Automated site-selection analytics using trial-history data, publication records, and patient-demographic overlays; Role-based dashboards for clinical-operations, medical-affairs, and regulatory teams; e
Consent integration and electronic trial-master file access for streamlined ethics-committee submissions; Secure messaging and document-annotation tools with audit trails; and Real-time performance metrics–enrollment rates, query resolutions, and site-tracker statuses. AI-driven study-site risk assessments flag protocol-deviation hotspots, enabling proactive mitigation. A compliance engine enforces 21 CFR Part 11 and GDPR requirements with policy-as-code and digital signature workflows. Sponsors leveraging VSI's IRM Portal see 25% faster site start-up timelines, 30% reduction in administrative overhead, and improved investigator satisfaction–accelerating trial execution while maintaining the highest standards of quality and compliance.
