Connect eligible patients with professional healthcare study partners through our regulatory-grade platform. 27% of patients no longer need to be excluded from life-changing clinical trials.
Trusted by leading pharmaceutical companies and CROs
Mental health clinical trials require patients to have study partners—but what happens when they don't have someone available? Critical research stalls, and patients miss life-changing opportunities.
Eligible patients are systematically excluded from potentially life-changing treatments simply because they lack a study partner, creating an equity barrier in clinical research.
Sponsors face extended timelines and millions in increased costs as studies struggle to meet recruitment targets, delaying breakthrough treatments from reaching the market.
Vulnerable populations without strong social networks are systematically excluded from research, limiting the generalizability of clinical trial results.
EMPAACT connects patients with professional healthcare study partners through our comprehensive, regulatory-compliant platform designed for clinical trial excellence.
Empowering every eligible patient to access clinical trials regardless of their personal support network, ensuring equitable participation in breakthrough research and removing social barriers to medical advancement.
Vetted healthcare professionals from our curated network provide reliable, trained support throughout the clinical trial journey, ensuring compliance and patient safety at every step.
Enterprise-grade technology capturing all interactions, managing complex logistics, and generating audit-ready datasets that sponsors and CROs need for regulatory submissions.
Simple, secure, and compliant integration that transforms your enrollment process in four straightforward steps.
Sites refer patients who need study partners through our secure portal, maintaining full HIPAA compliance and audit trails.
Our algorithm matches patients with qualified healthcare professionals based on location, availability, and clinical expertise.
Professional partners accompany patients to all required visits, providing consistent support throughout the trial duration.
Generate comprehensive reports and datasets that enhance your submission quality and provide valuable enrollment insights.
Join the pharmaceutical companies and CROs already using EMPAACT to accelerate trial timelines, reduce costs, and ensure equitable access to breakthrough treatments.