Automating Clinical Data Management with Lodol
In clinical trials, data is everything. From subject enrollment to adverse event reporting, every piece of information needs to be captured, validated, and transferred with precision. But for many research teams, Clinical Data Management (CDM) still relies heavily on manual processes and brittle systems.
Lodol brings modern AI-powered automation to clinical data workflows—helping research teams streamline operations, reduce delays, and ensure data integrity across the trial lifecycle.
Transforming Data Operations with Workflow Automation
Manual data entry, email-based case reviews, disconnected eCRFs, and spreadsheet trackers all slow down the pace of research. With Lodol, you can replace fragmented CDM steps with structured, automated flows—backed by audit trails and customizable checkpoints.
Our platform makes it easy to build logic-driven workflows that scale across study sites, sponsors, and regulatory systems—without sacrificing oversight or compliance.
Real-World Use Cases
- Data Entry Validation: Automatically review eCRF submissions for missing values, protocol violations, or query triggers before pushing to the EDC.
- Adverse Event Tracking: Route AE reports to clinical reviewers, notify safety teams, and generate regulatory submissions with versioned audit trails.
- Lab Data Reconciliation: Ingest lab reports from third-party providers, match them against subject schedules, and flag abnormalities for review.
- Query Management: Auto-generate data queries based on pre-defined rules, route them to sites, and escalate unresolved cases after configurable SLAs.
- Protocol Deviations: Detect unplanned visits or dosing anomalies and automatically route them to study leads for assessment and CAPA logging.
Deterministic, Reviewable, Compliant
Clinical workflows demand traceability and reproducibility. Lodol ensures every workflow behaves the same way, every time—backed by deterministic logic, human-readable steps, and complete audit histories.
Need a clinical reviewer in the loop? You can insert human approval steps wherever needed—ensuring that sensitive actions (like unblinding data or resolving SAE reports) get the review they require before progressing.
Built for Regulatory Rigor
With Lodol, every step of a workflow is version-controlled, testable, and exportable. Whether you're preparing for a sponsor audit or a regulatory inspection, your data operations are transparent by design—not just in hindsight.
We support integration with tools like Medidata Rave, Veeva Vault CDMS, OpenClinica, Google Sheets, and email—so your workflows stay connected to the systems your teams already use.
Faster Trials, Cleaner Data
With Lodol, your CDM team can move faster without sacrificing control. Automate the repeatable. Track the complex. Review what matters. Instead of drowning in spreadsheets and forms, your team can focus on ensuring quality data—and accelerating your path to submission.
Ready to modernize your clinical data workflows?
We’ll show you how Lodol can help you drive efficiency and quality across every stage of your clinical trials.