Signant Health

Signant Health is a clinical trial technology and services company dedicated to generating high-quality trial data for sponsors and CROs across the globe. With over 30 years of experience and thousands of trials supported, Signant Health provides comprehensive eClinical solutions, deep scientific expertise, and global operational support to help clinical teams extract clean, reliable data from patients and sites — for any trial, anywhere in the world.

Signant Health has played a role in clinical trials associated with 25% of novel drug approvals across the FDA and EMA from 2021 to 2024, making it a trusted partner for regulatory submissions and trial decisions. The company combines best-in-class technology with more than 50 in-house scientists and clinicians, attentive implementation teams, and mature project management to ensure trial integrity and simplify participation for both sites and patients.

Core eClinical Solutions

• eCOA/ePRO: Electronic clinical outcome assessment and patient-reported outcome tools designed to capture high-quality patient data throughout the trial lifecycle.
• Electronic Clinician Ratings: Digital solutions enabling structured, reliable clinician-administered assessments to support consistent data collection.
• EDC (Electronic Data Capture): A robust platform for capturing and managing clinical trial data with accuracy and efficiency.
• Unified eClinical Platform: An integrated suite that brings together multiple eClinical capabilities under one roof, giving sponsors and CROs ultimate control over their clinical data and intellectual property.
• RTSM (Randomization and Trial Supply Management): Technology to manage patient randomization and trial supply logistics seamlessly across global studies.
• Supply Chain Software: Tools providing end-to-end visibility and control over the clinical supply chain, from API to patient.

Key Capabilities and Expertise

• Solution: Full-featured, best-in-class eClinical solutions with zero capability gaps, ensuring sponsors have everything they need in a single platform.
• Science: Credible scientific and technical expertise to ensure trial integrity and deliver high-quality, reliable evidence, supported by 50+ in-house scientists and clinicians who assist with protocol design and measurement strategy from the earliest stages.
• Scale: Robust operational architecture and capacity to support global trials seamlessly, regardless of size or complexity.
• Service: High-quality, mature project management and dedicated support throughout the trial, with seasoned implementation teams that tailor recommendations to meet specific protocol requirements.

Experience and Track Record

• Over 30 years of experience in clinical trial technology and services.
• Thousands of trials supported across a wide range of therapeutic areas and geographies.
• Hundreds of drug approvals secured in partnership with sponsors and CROs.
• Associated with 25% of novel drug approvals across FDA and EMA from 2021 to 2024.
• Early-stage protocol guidance available through in-house scientific and clinical experts to shape measurement strategy and ensure data quality from the outset.
• Tailored implementation approaches designed to simplify site and patient participation while meeting unique protocol requirements.

Resources and Knowledge Sharing

• Signant Health offers a freely accessible resource hub including white papers, videos, case studies, and blog insights for clinical operations professionals.
• Notable resources include white papers on supply chain visibility and control, educational content on baseline score inflation detection and mitigation, and case studies such as streamlining global respiratory trial complexities with robust data capture strategies.

Signant Health serves as a comprehensive partner for sponsors and CROs seeking to simplify clinical trial execution, maintain data integrity, and accelerate the path to regulatory approval — all supported by decades of industry expertise and a full suite of integrated eClinical technologies.