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4-6 Week EDC Implementation vs. 12+ Week Industry Standard
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Stop waiting months for study startup. Get your clinical data flowing with the EDC system that deploys fast and adapts mid-study without downtime.

When regulatory timelines and funding milestones are at stake, you need more than fast implementation. You need an EDC partner with 25+ years of submission experience and zero tolerance for study disruptions.

 

Get Custom Study Analysis

Fast Implementation Backed by Clinical Expertise
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3,000+ studies completed means we've solved every implementation challenge you'll face.
Our clinical experts don't just build databases - they've guided submissions across oncology, CNS, and rare disease.

3,000+
STUDIES COMPLETED

83
COUNTRIES

100,000+
SITES SUPPORTED

25+
YEARS EXPERIENCE

When EDC Implementation Takes 3+ Months,
Your Entire Timeline Suffers
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Traditional EDC systems require lengthy custom builds and disruptive mid-study changes. Get the clinical data platform that deploys in 4-6 weeks and handles protocol amendments without system downtime or enrollment interruptions.

What Makes Signant's EDC Different?

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4-6 Week Implementation Speed

Modular eCRFs and streamlined edit checks accelerate setup while giving you full flexibility to use your own forms.

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Zero Downtime Protocol Changes

Mid-study protocol amendments are seamless - no interruptions, no downtime, and your data collection continues without a hitch.

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Clinical Experts Who Understand Your Therapeutic Area

Seasoned experts guide regulatory submissions across oncology, CNS, and rare disease, delivering the FDA-ready data your trial needs.

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Flexible eSource Integration

Mobile-responsive design enables direct data capture during patient visits, eliminating transcription errors and streamlining SDV workflows

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Risk-Based Monitoring Ready

Advanced tools for targeted SDV and remote monitoring that optimize resources while maintaining data quality and regulatory compliance

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24/7 Global Support When You Need It

Multilingual helpdesk and dedicated project managers across 83 countries - because clinical trials don't follow business hours

Accelerate EDC implementation. Get your free protocol review.

FAQs

Are you an eSource EDC?

Yes, our EDC supports eSource data collection. Our optional eSource capability is fully mobile enabled with a responsive design that enables clear and easy use on a tablet or smartphone – so investigators can use the solution during on-site consultations, and nurses can use it during home visits. Our solution enables the genealogy of data to be clearly identified – making it easy to distinguish data that is eSource and data that has been transcribed.​

Do you have an eCRF library?

Yes, our EDC comes with a comprehensive library of eCRFs, edit checks and custom functions. Our library speeds study builds by our project team, but the full library is also provided to self-service customers.

Do you support remote SDV?

Yes. Sites are able to upload source data evidence for remote review and sign off by the CRA. This speeds SDV activity, and reduces the amount of travel time CRAs need to expend.​

Do you build EDC studies for us?

Yes, at Signant we offer both full service and self-service EDC options.​

Can your EDC work alongside RBQM solutions?

Yes, our EDC makes it easy to define risk-based approaches to SDV, and to adjust these at the click of a button as the study progresses and the risk profile of each  individual site is understood.​

WHO IS SIGNANT HEALTH?

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Signant Health is the evidence generation company. We are focused on leveraging software, deep therapeutic and scientific knowledge, and operational expertise to consistently capture, aggregate, and reveal quality evidence for clinical studies across traditional, virtual, and hybrid trial models. For more than 25 years, over 600 sponsors and CROs of all sizes – including all Top 20 pharma – have trusted Signant solutions for remote and site-based eCOA, EDC, eConsent, RTSM, supply chain management, and data quality analytics.
Learn more at www.signanthealth.com.