MEET
OCR for Clinical Trials - ALCOA and 21 CFR Part 11 Compliant & Audit Ready
AI-powered OCR software for bio-pharma to digitize lab notebooks, submission forms, and trial data. Designed for ALCOA and 21 CFR Part 11 compliance and validated workflows that pass every audit.
21 CFR Part 11 Compliant OCR
ALCOA Principles Support
Validated OCR Workflows
Measurable ROI for Bio‑Pharma:
Reduce Data Entry Errors by 90% – Avoid costly mistakes in clinical trial documentation, lab reports, and regulatory submissions.
Accelerate Data Processing – Convert handwritten and printed trial records into searchable, structured formats in seconds.
Speed Up Regulatory Approvals – Ensure submission-ready documents faster, with fewer compliance roadblocks.
Compliance Without Compromise
21 CFR Part 11 OCR Software: Full audit trails, e-signatures, and robust data integrity controls.
ALCOA-Compliant Data Capture: Every data point is Attributable, Legible, Contemporaneous, Original, and Accurate.
Validated OCR Workflows for Bio-Pharma – Built to meet the most demanding trial documentation standards.
How It Works — Simple, Seamless Integration:
Upload your documents - lab notebooks, submission forms, or trial data files.
AI OCR Digitizes & Validates – Intelligent recognition ensures accuracy and compliance on every record.
Store, Share, Submit – Securely manage data with complete regulatory audit trails.
Social Proof & Testimonials
Trusted by Bio-Pharma Leaders — From Discovery to Regulatory Approval
See how clinical trial managers, QA officers, and R&D directors use Karla’s AI OCR to reduce errors, accelerate submissions, and achieve audit readiness with confidence.
"Implementing Karla’s AI OCR was a game-changer for our trial documentation. Error rates dropped by 90%, and our submission packages are audit-ready weeks earlier. In 20 years, I’ve rarely seen a technology deliver such an immediate impact."
"Before Karla, documentation was a bottleneck—prone to errors, delays, and last-minute compliance fixes. Now, turnaround is faster, accuracy is higher, and we’ve had zero audit findings in our last three inspections."
"Karla ensures every record we capture is ALCOA-compliant and 21 CFR Part 11–ready. For QA, that means no scrambling before audits—our data integrity is built in from day one."
Ready to Accelerate Your Clinical Trials with AI OCR?
See how Karla’s AI OCR for clinical trials delivers unmatched accuracy, compliance, and processing speed
