Regulatory submissions demand perfect data extraction. Every time.
Extract data from clinical trial documents, FDA submissions, and regulatory filings. Support drug development and compliance.
Pre-built templates ready to extract data from these document types.
Extract key data from clinical trial protocols and study designs...
Extract data from adverse event and pharmacovigilance reports...
Extract observations from FDA Form 483 inspection reports...
Extract data from pharmaceutical batch manufacturing records...
Extract data from pharmaceutical stability study reports...
Adverse event data scattered across batch records. 483 responses required weeks of manual data gathering. One late submission triggered an inspection.
Clinical data extracted and validated automatically. FDA responses compiled in days, not weeks. Our last inspection was routine.
— VP Regulatory Affairs, Biotech Company93%+ accuracy with confidence scores. Review uncertain fields before submission. Audit trails for regulatory traceability.
Extract data from batch records, adverse event reports, and clinical documentation. HIPAA-compliant processing available.
Process submission documents in hours instead of days. Meet FDA timelines without the scramble.
Processing 1,000+ documents monthly? Let's discuss your requirements.
P.S. The FDA doesn't accept 'we're working on it' as an answer.