Pharma & Life Sciences Document
Regulatory submissions demand perfect data extraction.
Extract key data from clinical trial protocols and study designs
No credit card required to get started.
Regulatory affairs teams manually extract data from clinical trial protocols and FDA correspondence. Compliance deadlines leave no room for error.
Structured output ready for your systems.
Upload your clinical trial protocol documents in PDF, image, or scanned format. Drag and drop or use our API.
Our AI identifies and extracts all 21 fields with 93%+ accuracy. No templates or training required.
Review extracted data with confidence scores. Approve, edit, or flag items for human verification.
Download as JSON, CSV, or Excel. Integrate via API or webhook to your existing systems.
Extract data for FDA submissions.
Process trial protocol documents.
Extract data from batch records.
Process adverse event reports.
Common questions about clinical trial protocol extraction.
We extract study ID, title, objectives, endpoints, design, and key inclusion/exclusion criteria.
Process amendments to maintain version history and track changes.
Treatment arms, dosing regimens, and visit schedules are extracted.
We extract data. Regulatory formatting and submission is your process.
Documents encrypted, processed in isolation, deleted after extraction.
Sign up for evaluation credits. Use redacted protocols for initial testing.
Our team processed hundreds of documents monthly by hand. Errors crept in, deadlines slipped, and skilled staff spent their time on data entry instead of strategic work.
Automated extraction changed everything. Same volume, processed in a fraction of the time. Our team finally focuses on what matters.
— Operations Director, Enterprise CompanyProcessing 1,000+ documents monthly? Let's discuss your requirements.
No credit card required to get started.
P.S. The first 10 documents are on us. See for yourself.
