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Fortrea
About CRO
Contract research organization spun off from Labcorp, providing Phase I-IV clinical trial management, patient access solutions, and regulatory services.
Technology & Expertise
At Fortrea, we specialize in Clinical Operations & Trial Management, Patient Recruitment & Retention, Regulatory Affairs & Submissions, Data Management & Biostatistics. Our approach brings together study start-up, cross-functional trial oversight, and operational delivery; patient identification, enrollment planning, engagement, and retention; regulatory strategy, dossier development, submission management, and authority support; and connected specialist capabilities, enabling project teams to scale support as priorities and development stages change.
Core Services
Our service portfolio spans Clinical Operations & Trial Management, Patient Recruitment & Retention, Regulatory Affairs & Submissions, Data Management & Biostatistics. Fortrea can coordinate feasibility, project management, site coordination, and study close-out; recruitment strategy, outreach, screening support, and participant engagement; planning and delivery of regulatory documents across development milestones; and connected specialist capabilities within a defined project structure designed around milestones, data needs, and operational priorities.
Accreditations & Compliance
At Fortrea, the compliance package is aligned with the proposed scope of work. Accreditation status, regulatory coverage, and inspection evidence should be confirmed for the exact facility and service included in the proposal.
