Comprehensive Site Management Capabilities

Discover MedPath’s full-service SMO capabilities, including CTMS with eSource, eRegulatory, eConsent, and eDOC for seamless trial execution

Our Capabilities

Empowering clinical research through advanced technology and expert coordination

Infogram of a medical staff looking the screens with dashboards on a computer

Patient Recruitment & Retention

Multi-channel strategies, community engagement.

Regulatory & Ethics Management

IRB coordination, documentation, submissions.

Clinical Operations Support

Site setup, coordination, monitoring

CTMS Platform

Centralized CTMS platform featuring:

eSource (paperless data collection)
eRegulatory (document management)
eConsent (secure digital consent)
eDOC (central document storage)

Start Your Next Clinical Trial

Connect with our experienced team to discuss your research needs and discover how our multi-site capabilities, digital infrastructure, and therapeutic expertise can accelerate your study success.

Get Started Today