Pharmaceutical Innovation Management

KanBo acts as a digital innovation and compliance hub, helping the pharmaceutical organization unify global teams, structure workflows, and adapt quickly to dynamic regulatory and market conditions. Key functional areas include:

I. AI-Driven Drug Discovery Management

  • Research Boards: Track milestones, hypotheses, and experiments.
  • AI Progress Dashboards: Visualize machine learning workflows and discoveries.
  • Task Automation: Streamline repetitive tasks and manage dependencies.

II. Regulatory Compliance & Risk Alignment

  • Compliance Spaces: Centralize FDA/EMA documentation and SOPs.
  • Approval Workflows: Ensure timely reviews and submission tracking.
  • Notification Systems: Alert teams to regulatory updates and deadlines.

III. Clinical Trial Coordination

  • Trial Phase Boards: Manage preclinical through Phase IV.
  • Enrollment Tracking: Monitor patient recruitment and retention.
  • Analytics Integration: Real-time trial data, adverse event tracking, and KPIs.

IV. Market Expansion & Global Strategy

  • Market Entry Playbooks: Assess timelines, partners, and market access risks.
  • Expansion Cards: Track country-specific requirements and legal status.
  • Strategic Maps: Visualize go-to-market activities and expansion milestones.

V. Direct-to-Consumer (DTC) Engagement

  • Patient Journey Boards: Coordinate engagement, education, and support.
  • Telehealth Scheduling Tools: Manage appointments and follow-ups.
  • Delivery Coordination: Track last-mile medication logistics and feedback loops.

VI. Resource Allocation & R&D Optimization

  • Project Workload Views: Identify resource bottlenecks across departments.
  • Budget Tracking Cards: Align costs with ROI-focused initiatives.
  • Strategic Dashboards: Optimize time and talent allocation across pipelines.

Month 1 – Planning and Setup

Months 2-6 – Pilot Phase

Month 7 – Pilot Evaluation

Months 8-18 – Full Rollout