
Target Health
Clinical trial software and full-service CRO for drug, biologic, and device development with real-time data management and eSource capabilities.
Overview
Target Health is a full-service contract research organization (CRO) and clinical trials software company serving the pharmaceutical, biologic, and medical device development community. The company combines clinical research services with proprietary eSource software to support paperless clinical trials, offering clients an integrated approach to study management, data handling, regulatory submissions, and project oversight.
Target Health operates a Global Partnership network (the Target Health Global Partnership, or THGP), which brings together small to mid-size companies from around the world to provide experienced approaches to drug, biologic, and device development. To date, more than 1,000 studies have been conducted globally using the Target Clinical Trial Software System, over 40 drugs and devices supported by the Target Software Suite have received regulatory approval across the US, Canada, EU, and Japan, and approximately 90% of data in studies run on the eSource platform is entered in real time.
Clinical Research Services
- Personalized clinical and project management services tailored to individual study needs
- Full-service clinical research support aimed at increasing the probability of product success
- Global study execution across multiple therapeutic areas and product types, including drugs, biologics, and devices
Data Services
- Data management services designed to deliver reliable outcomes
- Biostatistical services integrated with data management workflows
- Real-time data access to support risk-based monitoring (RBM) and faster decision-making
- Capability to merge non-CRF data with CRF data and include combined datasets in reports
Software — eSource and Clinical Trial Software Suite
- Proprietary eSource software enabling paperless clinical trials
- Positioned as an efficient and cost-effective alternative to conventional paper-based trials
- Supports the full data lifecycle from data entry and query management through to database lock and final Clinical Study Reports (CSR)
- Approximately 90% of data entered in real time in studies using the eSource platform
- Clients report improvements in overall data quality, data integrity, and significant cost and time savings compared to paper-based approaches
Regulatory Services
- Regulatory support services focused on increasing the speed and reliability of the approval process
- Track record of supporting approvals from regulatory agencies in the US, Canada, EU, and Japan
Global Partnerships and Clients
- The Target Health Global Partnership (THGP) connects small to mid-size CROs and service providers worldwide
- Partnership model is designed to offer sophisticated and experienced approaches to development across geographies
- Target Health participates in international industry events, including Medica 2025
Target Health serves pharmaceutical and life sciences organizations seeking an integrated CRO and software partner, with a particular emphasis on real-time data access, paperless trial execution, and end-to-end support from study initiation through regulatory approval.