ABOUT US
Who Is Signant Health?
The best technology succeeds in the background. Signant Health provides solutions that simplify every step of the patient journey to make it easier for people to participate in, and for sites and study teams to run, clinical trials. Signant unites eCOA, eConsent, Patient Engagement, IRT, Clinical Supplies and Endpoint Quality into the industry’s most comprehensive patient-centric suite – an evolution built on more than 20 years of proven clinical research technology. Our intense focus on the patient experience, deep therapeutic area expertise and global operational scale enable hundreds of sponsors and CROs (including all Top 20 pharma) to extend the reach of drug development, expand patient opportunities and improve data quality – helping them bring life-changing therapies to our families and communities around the world. Take a significant step toward patient-centricity at signanthealth.com.
CRF Health and Bracket are now Signant Health
CONTACT INFORMATION
Signant Health
4000 Chemical Road, Suite 400
Plymouth Meeting, PA 19462
UNITED STATES
Phone: 267 498 2300
Fax: 215 565 0001
Contact: Heather Bilinski
FEATURED ARTICLES
- Signant Health Enhances Audit Trail Reporting Capabilities In TrialMax® To Improve eCOA Data Integrity Monitoring
- Learnings On Bring Your Own Device Uptake For eCOA Implementation
- Operating System Upgrades Do Not Adversely Affect eCOA Completion Behavior
- Can Older Users Use Electronic Clinical Outcome Assessments?
- CRF Health Industry Luminaries To Share eSource Expertise In Clinical Trials At DIA 2018
- Recognition For CRF Health’s World Class eSource Wins European Award
- Monitoring Clinical Trials With Electronic Informed Consent
- Validating Clinical Trial Data: Paper vs. eCOA
- Can eCOA Be Used For Pediatric Clinical Trials?
- Tips For Implementing An eConsent Solution
- How To Select The Most Effective eCOA Modality For Your Study
- Translations and eConsent
- 14 Drivers Of eConsent Adoption In Clinical Trials – Infographic
- How eConsent Improves Consent Development
- The Value Of Electronic Informed Consent
- Reducing Regulatory Risk In Clinical Trials With eConsent
- 3 Major Regulatory Risks You Can Reduce With Electronic Informed Consent
- Recruiting And Retaining Patients With eConsent
- How To Calculate The True Cost Of Paper When Considering eCOA
- Six Tips For The Successful Integration Of Econsent
- Paper To eCOA: A Guide To Migration
- How Electronic Data Collection Helps Meet The FDA's Quality Guidelines
- How To Select The Most Effective Modality For Your eCOA Study
- eCOA Essentials: 1 Hour To Higher Quality Data
- eCOA Design and Implementation Overview
- Electronic Clinical Outcome Assessments (eCOA): An Introductory Guide
- eCOA And Equivalence Testing: New Evidence From Meta-Analysis
- 10 Insider Tips For eCOA Implementation
- The Challenges Of Paper Backups In eCOA Studies
- The Hidden Costs Of Paper-Based Clinical Outcome Assessments
- Managing eCOA Device Allocation And Resupply In Clinical Trials
- Using eCOA To Overcome Data Collection Challenges In Oncology Trials
- Clinical Trials In Oncology: A Patient's Perspective
- Clinical Trials In Diabetes: Best Practices For The Collection Of Electronic Patient Data