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
![The FDA issued a draft guidance in September 2018 to detail the regulatory body’s thinking on monetary penalties of up to $10,000 per day for failing to register a clinical trial, patterns of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 Zach Weingarden, Product Solutions Manager, TrialAssure, helps clarify some common questions on this draft guidance that sponsors and other partners have been asking.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](https://www.trialassure.com/wp-content/uploads/2019/06/26.-Common-clinical-trial-transparency-questions-answered-scaled-e1594058165442.jpg)
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.