Artificial intelligence that amplifies pharmaceutical expertise — accelerating every deliverable while preserving the scientific rigour and regulatory compliance your products demand.
What took weeks now takes days. AI accelerates first drafts, evidence synthesis, and routine tasks — freeing your experts for strategic work.
Every AI output is reviewed by qualified pharmaceutical physicians, PhD scientists, and regulatory specialists before it reaches you. No exceptions.
Built around ABPI, EFPIA, PhRMA, and FDA/EMA requirements from day one. Full audit trails, version control, and regulatory-grade documentation.
Every deliverable follows a structured process that combines AI acceleration with rigorous expert oversight.
Senior experts define the strategic approach, audience, and compliance requirements for your project.
AI generates structured first drafts, evidence summaries, and content frameworks at speed.
Pharmaceutical physicians and medical writers refine content for scientific accuracy, strategic alignment, and brand voice.
ABPI Final Signatory review and MLR-readiness checks. Reference verification and fair balance assessment.
Final deliverables with full audit trail. Rapid iteration cycles for feedback and revisions.
Real performance comparisons across common Medical Affairs and Medico-Marketing deliverables.
How AI accelerates delivery across Medical Affairs, evidence generation, medico-marketing, and market access — without compromising scientific quality.
Automated tracking of publications, congress presentations, and emerging data across your therapeutic areas. AI surfaces what matters — your experts decide what it means.
AI generates structured first drafts following your style guides, templates, and brand voice. Medical writers then refine for scientific accuracy and strategic nuance.
Automated reference checking, cross-document consistency verification, and regulatory screening. Catches issues before MLR — not during.
Data-driven intelligence that informs medical strategy, KOL engagement, and channel optimisation. Actionable insights, not raw data dumps.
Streamline the operational burden of Medical Affairs and Marketing. Automated routing, version control, feedback consolidation, and approval tracking.
Handle concurrent projects across therapeutic areas and geographies. Maintain quality during peak periods — launches, congresses, regulatory milestones.
Real-world impact across pharmaceutical and biotech clients
Enterprise-grade security, full transparency, and human oversight at every stage. Your data never enters public AI systems.
Your proprietary data stays private. Enterprise-grade infrastructure with zero public AI exposure.
Full visibility into how AI is used across every deliverable.
Every AI output receives rigorous expert validation before delivery.
Active measures to prevent and detect algorithmic bias across all outputs.
See how AI-enhanced Medical Affairs and Medico-Marketing can accelerate your timelines while elevating quality. We'll show you exactly how it works on your deliverables.