Register and submit clinical trial information across global registries from a single source of truth
Capture, manage, and submit study information efficiently across global registries
Built-in compliance tracking and automated workflows to ensure every requirement is met
One centralized solution to register and submit clinical trial data faster, more accurately, and with confidence.
Cut the time from data capture to submission-ready with AI-assisted tools and a unified form that eliminates duplicate entry across registries.
AI Importer maps unstructured data to Study and Form fields, reducing manual effort and accelerating submission readiness.
Global Disclosure Form eliminates duplicate data entry across registries, reduces compliance risk, and streamlines global submissions.
Workflows and a flexible rules engine help teams track obligations, enforce policies, and maintain audit readiness at every step.
Automated, customizable workflows help teams manage, track, and assess disclosure activities while supporting audit readiness and compliance.
Rules Creator helps you build flexible rules to enforce global regulations and company-specific policies, ensuring requirements are met with confidence.
Stay in control of your global disclosure program with reporting dashboards and integrations that connect your systems and surface compliance status in real time.
Reporting dashboards provide visibility into disclosure tracking, compliance status, and operational efficiency across your portfolio.
APIs and integrations connect internal systems, automate data exchange, and streamline disclosure processes across your organization.
Maps unstructured source data to Study and Form fields automatically, dramatically reducing manual effort and time to submission readiness.
A single unified form that eliminates duplicate data entry across registries and reduces compliance risk on global submissions.
Build and test flexible, company-specific policy rules across registries to ensure every requirement is met with consistency and confidence.
Customizable workflows manage, track, and assess disclosure activities across your team — supporting audit readiness at every stage.
Real-time visibility into disclosure tracking, compliance status, and operational efficiency across your entire trial portfolio.
Connect internal systems, automate data exchange, and streamline disclosure processes across your organization's existing infrastructure.
The AI Importer automatically maps unstructured data — from protocols, synopses, and other source documents — directly to Study and Form fields, cutting manual preparation time and getting you to submission-ready faster.
The Global Disclosure Form captures study data once and maps it across multiple registries simultaneously, eliminating duplicate entry, reducing inconsistency, and lowering the risk of non-compliance at scale.
Rules Creator lets you define and test company-specific policy rules alongside global regulatory requirements — so your teams always know whether a disclosure meets the standard before it’s submitted.
Automated workflows and a full activity log ensure every action is tracked, every requirement is documented, and every submission is backed by a complete, reviewable audit trail.
Speak to a Citeline expert to discuss your use case, access needs, and the right setup for your organization.
TrialScope Disclose is the industry’s most trusted clinical trial disclosure management solution, helping sponsors register and submit trial information across global registries from protocol planning through results submission — from a single centralized platform.
The AI Importer automatically maps data from unstructured source documents — such as protocols and synopses — directly to Study and Form fields within TrialScope Disclose, significantly reducing manual data entry and accelerating submission readiness.
The Global Disclosure Form is a unified data entry interface that captures study information once and maps it across multiple registries simultaneously, eliminating duplicate entry, reducing errors, and streamlining global submissions.
Rules Creator allows teams to build and test flexible rules that enforce both global regulatory requirements and company-specific policies across registries — ensuring disclosures meet the required standard before they are submitted.
TrialScope Disclose supports submission to a broad range of global registries including ClinicalTrials.gov, EU CTR, ISRCTN, PMDA, ANZCTR, and many others, with ongoing updates as registry requirements evolve.
Automated workflows maintain a full activity log of every action taken in the system, ensuring all disclosure activities are tracked, documented, and reviewable — so teams are always prepared for internal or regulatory audit.
Yes. TrialScope Disclose provides APIs and integration capabilities that connect with internal clinical and regulatory systems, automating data exchange and embedding disclosure workflows into your existing infrastructure.
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