Contract intelligence for Life Sciences
Docfide understands clinical trial agreements, research collaborations, and licensing deals. Built for the complexity of biotech and pharma contracting.
Clinical trial agreements that don't slow you down.
CTAs are high-volume, high-stakes, and every site wants something different. Docfide automates the routine, flags the exceptions, and keeps your trials on schedule.
Protocol-Aware Review
AI understands study phases, IND/IDE requirements, and protocol-specific terms. Flags non-standard provisions against your playbook automatically.
Publication & Data Rights
Manage publication provisions, data ownership, and disclosure restrictions across investigator agreements. Never lose track of who owns what.
Site & Enrollment Management
Track enrollment targets, site activation status, and CTA amendments in real time. Know which sites are signed and which are stalling.
Licensing deals structured for the long term.
Royalty calculations, milestone payments, and field-of-use restrictions require precision. Docfide ensures every deal is structured correctly from the start.
Royalty & Milestone Intelligence
Track milestone payments, running royalties, and sales-based earn-outs automatically. Get alerts when obligations are due.
IP & Patent Management
Define background IP, manage patent prosecution obligations, and enforce field-of-use restrictions. No ambiguity about who owns what.
Diligence Obligation Tracking
Monitor commercially reasonable efforts clauses, development milestones, and sublicensing reporting requirements across your portfolio.
Regulatory compliance baked into every contract.
FDA inspections, EMA submissions, and ICH-GCP compliance. Your contracts need to hold up to regulatory scrutiny. Docfide ensures they do.
FDA/EMA/ICH-GCP Compliance
Pre-built clause libraries aligned with regulatory standards. Automated checks ensure your CTAs and licensing deals comply with applicable regulations.
Regulatory Submission Tracking
Track regulatory submission deadlines, IND/CTA filings, and approval contingencies. Never miss a filing window.
Audit-Ready Documentation
Complete audit trails for every contract change, approval, and signature. Ready for FDA inspection at a moment's notice.
Solutions for every life sciences use case
From early-stage research to commercial launch, Docfide adapts to your contracting needs.
Built for the rigor of life sciences.
From CTAs to licensing deals, Docfide handles the complexity so you can focus on bringing therapies to patients.