Pharmaceutical AI Agent Suite
Pharma AI that works inside your PDFs, Word, Excel & PowerPoint
Review with AI highlights and comments in the PDF viewer. Draft in Word with tracked changes. QC spreadsheets and generate slides in your native formats—no file conversions, no copy-paste to a chat, and guardrails aligned to life-sciences workflows.
AI-annotated PDF reviews
The agent reviews your existing PDFs and leaves highlights and threaded comments directly in the viewer—pinning every finding to the exact page, table, and line instead of a separate chat summary.
Side-panel threads, reviewer assignments, and mentions in context
Delta & discrepancy highlights vs. prior versions and source tables
One-click audit pack export with all markups and evidence links
Clinical data validation & trending
Run SOP-aligned edit checks, anomaly detection, and investigator-ready summaries on study workbooks—no copy/paste, no reformatting.
Automated edit checks mapped to study and PV rules
Trending & outlier alerts when thresholds are breached
Instant exports for statistician and safety sign-off
Medical affairs narrative creation
Generate slides directly into your approved templates with citations and claim governance—ready for MLR, KOL briefings, and launch enablement.
Template library aligned to approved messaging frameworks
Automatic insertion of citations and claim references
Workflow gates for medical, legal, and regulatory approval
Procedure & response drafting
Edit Word files directly with tracked changes—keeping headings, tables, cross-refs, and styles intact. Draft SOPs, CAPA responses, and clinical summaries with inline citations.
Tracked-change drafting that respects your template & styles
Inline citation and reference management from approved sources
Version-controlled redlines with approval checkpoints
Platform Overview
Purpose-built for pharmaceutical velocity and compliance—without changing tools
Deploy PDF Annotate, Excel Analysis, PowerPoint Narrative, and Word Authoring Agents together. Keep reviewers in the loop while eliminating the manual copy-paste and re-formatting that slow filings, approvals, and launches.
Works inside your documents
PDF agent annotates the current file with highlights & comments. Word/Excel/PowerPoint agents edit native files—tracked changes, formulas, and templates preserved.
Grounded & traceable outputs
RAG plus structured templates ensure every note, calculation, slide, and paragraph points back to a validated source or exact PDF coordinate.
Pharma-grade control points
Role-based approvals, version locks, and export archives align to GxP practices and FDA 21 CFR Part 11 expectations for validation and auditability.
Agent Catalog
PDF, Excel, PowerPoint, and Word agents aligned to pharmaceutical workstreams
Each agent keeps work in its native format with the guardrails RA, QA, medical, and commercial teams expect— so adoption is fast and validation stays straightforward.
PDF Annotate Agent
AI reviews your PDF and writes highlights & threaded comments directly in the viewer—so findings are visible where reviewers actually look.
Pin findings to exact pages, figures, and table cells.
Dual-pane comparisons for label updates and protocol deltas.
Reviewer assignments, mentions, and exportable audit packs.
Excel Analysis Agent
Automate QC, validation, and anomaly detection across complex study workbooks and PV trackers.
Edit checks mapped to study SOPs and data models.
Outlier detection & trending tuned for life-sciences KPIs.
Change tracking with approval checkpoints for GxP teams.
PowerPoint Narrative Agent
Compose slides in your approved template with citations and governed claims—ready for MLR and field enablement.
Controlled templates aligned to medical, legal, and regulatory standards.
Auto-inserted citations and claims with references.
Multi-team review checkpoints before publishing.
Word Authoring Agent
Draft and revise DOCX directly with tracked changes—keeping headings, tables, and cross-references intact.
Context-aware drafting with inline citation management.
Structured change history to accelerate reviews.
Embedded compliance checklists tied to internal SOPs.
Use Cases
Designed for every step of the molecule-to-market journey
Start with the agent that meets today’s need—or orchestrate them together to remove manual reviews and accelerate submissions, approvals, and launches.
Regulatory affairs
Accelerate dossier prep, labeling change control, and health-authority Q&A with PDF annotations and Word redlines ready for submission.
Agents: PDF Annotate Agent, Word Authoring Agent
Clinical development
Automate protocol deviation checks, site communications, and safety narratives while maintaining oversight in native files.
Agents: PDF Annotate Agent, Excel Analysis Agent, Word Authoring Agent
Medical affairs
Produce compliant medical content, KOL briefing packs, and insight reporting using claim-governed PowerPoint and cited Word sections.
Agents: PowerPoint Narrative Agent, Word Authoring Agent
Commercial operations
Generate promotional materials with approved claims, monitor feedback, and stay aligned with medical/legal standards.
Agents: PowerPoint Narrative Agent, Excel Analysis Agent
Security & Governance
Built to meet life-sciences compliance requirements
Each agent inherits your existing controls, keeping sensitive IP and patient data protected while delivering AI-powered productivity your teams can audit.
Isolated deployments for PDF, Excel, PowerPoint, and Word agents with SOC 2 controls and configurable data residency.
Versioned audit trails spanning annotated PDFs, validated spreadsheets, approved decks, and authored documents.
Governance guardrails per agent—redaction, prompt filtering, and response validation with role-based access.
Ready to accelerate?
See the pharmaceutical agent platform in action
Schedule a tailored walkthrough of the PDF Annotate, Excel Analysis, PowerPoint Narrative, and Word Authoring Agents to see how the full suite accelerates compliant pharmaceutical workflows.
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