Simplify clinical trial registration and results disclosure

TrialAssure REGISTRY® is a start-to-finish e-registration tool for creating, filing, and managing clinical trial registrations and results disclosure around the globe.

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All registries handled with one portal

Reduce your trial registration and disclosure workload and consolidate obligations to multiple global trial registries with one system.

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Stay ahead of ClinicalTrial.gov record update deadlines

30 days

Deadline to update ClinicalTrials.gov record when investigational site closes

EMA launching date for a new clinical trial registry platform

2022

Scheduled release of new EMA registry platform with new requirements

21-day protocol registration with TrialAssure REGISTRY

50%

Improvement in meeting 21-day protocol registration target with TrialAssure REGISTRY

Tame the trial registration chaos

Streamline deliverables

REGISTRY® puts a complete registration and disclosure toolset at your fingertips.

Integrate with your CTMS, data warehouse, or other sources to complete registrations and disclosures.
Use form-based data entry to tailor outputs for dozens of registries worldwide.
Tap a single data record and file electronically to multiple registries.
Receive immediate feedback on missing or out-of-compliance elements.

Register trials anywhere on Earth

The REGISTRY® rules engine reflects the requirements of nearly 40 major registries, including ClinicalTrials.gov, EudraCT, and numerous national registries.

Rules are continually updated by TrialAssure’s transparency experts to keep pace with changing registry requirements, allowing you to remain compliant in a constantly evolving landscape.

Configure and manage workflows

Oversee clinical trial registration and results postings and augment built-in regulatory intelligence with your organization’s own processes and custom registries. Intuitive dashboards show workflow steps and track the status of each study.

Registry assessment
Validation
Quality checks
Review cycles
Approvals
Regulatory authority comments

An innovative registration and disclosure solution

Turn to TrialAssure’s transparency experts to ensure that the latest updates and needs in global clinical trial registration and results disclosures are covered. Our software can handle intricate, multi-step workflows and adapt to your requirements and roles with ease.

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The FDA issued a draft guidance in September 2018 to detail the regulatory body’s thinking on monetary penalties of up to $10,000 per day for failing to register a clinical trial, patterns of previous noncompliance, and/or submitting misleading or false information to ClinicalTrials.gov. While the FDA has not previously begun issuing fines to pharmaceutical companies, this guidance brings that reality one step closer. Zach Weingarden, Product Solutions Manager, TrialAssure, helps clarify some common questions on this draft guidance that sponsors and other partners have been asking. Zach Weingarden, Product Solutions Manager, TrialAssure

How TrialAssure Gathers Client Feedback to Build Stronger Clinical Trial Transparency Software

We value sponsor feedback

It may not sound revolutionary, but simply listening to our clients to build stronger clinical trial transparency software is the foundation for effective innovation.

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