Eclaire transforms the clinical trial validation process with autonomous agents that generate and execute test cases across EDC systems like Veeva, reducing validation time from months to days.
Eclaire transforms a tedious, error-prone process into a rapid, autonomous operation that reduces validation time from 60-90 days to just 2 days.
Reduce validation time from 60-90 days to just 2 days with AI-powered automation, dramatically accelerating your trial timelines.
Our AI autonomously creates positive, negative, and edge test cases that ensure comprehensive EDC system validation.
Drastically reduce resource requirements from 3-5 FTEs to just 0.5 FTE, cutting operational costs while improving quality.
Eclaire's platform seamlessly integrates with your EDC systems like Veeva to automate the entire edit check validation workflow, eliminating manual processes and accelerating timelines.
Eclaire connects directly to your EDC systems like Veeva, Medidata, and Oracle Clinical, automatically extracting edit check logic, validation rules, and form designs without disrupting your existing infrastructure.
Our proprietary AI engine analyzes your study specifications and automatically generates comprehensive test cases that cover all validation scenarios – positive, negative, edge cases – without human intervention.
Eclaire executes thousands of test cases simultaneously across your EDC environment, completing in hours what would traditionally take weeks of manual testing, while maintaining detailed evidence for regulatory compliance.
Monitor validation progress, view test results, and identify potential issues through our intuitive dashboard. Get automatic alerts for failures and track key metrics like completion rates, coverage, and validation health score.
Eclaire automatically generates comprehensive validation documentation including test evidence, traceability matrices, and regulatory-ready reports that satisfy FDA, EMA, and ICH requirements for audit trails and compliance.
Our reinforcement learning algorithms continuously improve test cases based on execution results, adapting to changes in your EDC system and study design, and automatically updating when specifications change.
Eclaire's AI-powered edit check validation delivers significant benefits across your entire clinical trial lifecycle, from accelerated study startup to early database lock.
Reduce study build and validation from 90 days to just 2 days, allowing trials to begin collecting patient data significantly earlier and accelerating your entire development timeline.
Comprehensive validation ensures edit checks function correctly from day one, dramatically reducing data queries, protocol deviations, and the need for database corrections during the trial.
Reduce staffing needs from 3-5 FTEs to just 0.5 FTE for edit check validation, allowing your expert team to focus on higher-value activities instead of repetitive testing tasks.
When protocol amendments require edit check changes, Eclaire automatically validates the updates within hours instead of weeks, minimizing disruption to ongoing trials and data collection.
Higher data quality throughout the trial results in fewer queries at study close, enabling earlier database lock, faster analysis, and quicker submission to regulatory authorities.
Through accelerated timelines, reduced resource requirements, and improved data quality, sponsors achieve an average of $2.4M in direct cost savings per trial, with additional market advantages from earlier product launches.
Eliminate the burden of manual test case creation and execution, allowing data managers to focus on optimizing data collection strategies and implementing more effective edit checks.
Accelerate study startup timelines, reduce operational bottlenecks, and improve site and patient experience through properly functioning edit checks that minimize data queries.
Transform testers' roles from repetitive execution to strategic oversight, allowing them to focus on test strategy, edge cases, and continuous improvement rather than manual testing.
Achieve significant cost savings, accelerate time-to-market, and improve resource allocation while maintaining the highest standards of data quality and regulatory compliance.
Ensure comprehensive validation coverage with detailed documentation and audit trails that exceed regulatory requirements while dramatically reducing the risk of validation errors.
Accelerate the development of life-saving treatments by reducing trial timelines, improving data quality, and bringing critical therapies to market faster for patients in need.
Leading pharmaceutical companies and research organizations are transforming their clinical trial operations with Eclaire's AI-powered edit check validation.
"Eclaire revolutionized our validation process. What used to take our team of 4 people nearly three months now completes in just 48 hours with minimal oversight. Beyond the obvious time and cost savings, we've seen a significant improvement in data quality and a 64% reduction in data queries. This technology is transforming how we approach clinical trials."
"As a CRO supporting multiple concurrent trials, the ability to rapidly validate edit checks with Eclaire has been a game-changer. We've reduced our validation resources by 85% while improving quality and consistency. The self-healing test cases adapt automatically to specification changes, which has been invaluable during mid-study amendments. The ROI was evident within the first month."
"For our Phase III oncology trial with complex edit checks across 200+ sites, traditional validation would have taken months and delayed our timeline significantly. With Eclaire, we validated over 3,000 test cases in parallel within 36 hours, identified 28 critical issues that would have caused downstream problems, and launched on schedule. The platform paid for itself multiple times over."
Choose the plan that best fits your clinical trial validation needs and budget, with options for organizations of all sizes.
For smaller research teams and early-phase trials
For mid-sized organizations managing multiple trials
For large organizations with complex validation needs
Join industry leaders who are saving months of development time and millions in costs while improving data quality with Eclaire's AI-powered edit check validation platform.