90-Day Roadmap

Claude AI Pharmaceuticals & Life Sciences Implementation Guide

The exact roadmap we use with our pharmaceuticals & life sciences clients — from first stakeholder call to measurable ROI in 90 days. No fluff, no delays, no surprises.

✓ Foundation
✓ Pilot
→ Scale
Phase 01

Foundation (Days 1–30)

  • GxP compliance assessment
  • 21 CFR Part 11 validation protocol
  • Regulatory affairs team engagement
  • Pilot submission type selection (literature reviews)
  • Qualified Person review framework
Phase 02

Pilot (Days 31–60)

  • Literature review automation pilot
  • CSR summary generation (non-submission)
  • Scientific quality review process
  • Accuracy benchmarking vs manual
  • Regulatory agency communication strategy
Phase 03

Scale (Days 61–90)

  • CTD section drafting pilot
  • Pharmacovigilance integration
  • Medical affairs content automation
  • Full validation package completion
  • ROI report to Chief Scientific Officer

Success Metrics by Phase

Phase 1 Metrics

  • Stakeholder sign-off achieved
  • Pilot scope defined
  • Integration tested

Phase 2 Metrics

  • First output quality score >85%
  • Team adoption >80%
  • Baseline metrics captured

Phase 3 Metrics

  • ROI measured and documented
  • Organisation-wide rollout complete
  • Phase 2 roadmap approved

ClaudeReadiness Implementation Support

You do not have to follow this roadmap alone. Our team has delivered 200+ Claude implementations in pharmaceuticals & life sciences and adjacent industries. We provide hands-on programme management, technical integration support, and change management from day one to day 90.

Start Your 90-Day Programme Our Implementation Service
The Claude Bulletin

Weekly Claude deployment intelligence

3,000+ enterprise leaders read it every week. Join them.