Search life sciences software.

by Medidata

Electronic clinical outcome assessment for faster study builds, patient engagement, and real-time data quality insights.

by Medidata

Unified patient portal for clinical trials integrating consent, eCOA, payments, and visit tracking in one experience.

by Medidata

Digital informed consent and enrollment management for clinical trials, with adaptive workflows for pediatric studies and real-time site oversight.

by Medidata

Continuous medical-grade data capture combining objective digital measures with eCOA for clinical trials, generating endpoint-ready evidence without increasing patient burden.

by Medidata

Automated trial participant reimbursement linked to study activity, reducing site burden and payment delays.

by Medidata

Patient registry and portal for pre-trial recruitment, ongoing engagement, and post-trial follow-up in clinical research.

by Medidata

AI-powered protocol evaluation using cross-industry trial data to identify design risks, predict enrollment and retention impact, and reduce protocol amendments.

by Medidata

Structured endpoint review and adjudication for clinical trials, with traceable decisions, committee workflows, and audit-ready documentation.

by Medidata

Risk-based source data verification for clinical trials, focusing verification on critical safety and efficacy data to reduce monitoring costs.

by Medidata

AI-powered enrollment forecasting, site selection, and diversity analytics for clinical trial feasibility planning.

by Inovalon

Real-world data analytics for clinical trial site selection, patient recruitment, and diversity planning.

by Inovalon

Automated patient eligibility screening and recruitment for clinical trials using EHR data and AI-powered matching.

by Inovalon

Real-time patient eligibility assessment for clinical trials using longitudinal claims data and medical history.

by Advarra

AI-powered operational intelligence for clinical trial design, planning, and conduct—extracting actionable insights from trial data across the entire lifecycle.

by Advarra

Clinical trial management for academic medical centers and cancer centers, covering protocol oversight, participant tracking, billing compliance, and financial management.

by Advarra

Clinical trial management, enrollment, and financial operations for research sites and health systems.

by Advarra

21 CFR Part 11-compliant document management and routing for regulatory workflows across research sites.

by Advarra

Electronic source data capture and management for clinical trial sites with 21 CFR Part 11 compliance and remote monitoring.

by Advarra

Data-driven protocol design and feasibility insights for clinical trials, powered by operational data from 30,000+ studies.

by Advarra

Clinical trial site selection using IRB-backed performance data and streamlined feasibility assessments for sponsors and CROs.