Move to Life Sciences Autonomy
Replace document-heavy healthcare and pharmaceutical operations with governed AI workflows that execute across teams, systems, and regulated processes.
Time lost to documentation - ScienceDirect
AI embedded in health operations - McKinsey
Up to 97% faster documentation draft with AI
↘ Manual work
Document-driven work
Manual authoring, reviews, and approvals
Fragmented compliance processes
Rework caused by missing or inconsistent data
High audit and inspection preparation burden
Slow submissions, and delayed approvals
Reactive care, and bottlenecks
↗ Autonomous work
Structured, event-driven regulated workflows
AI-assisted authoring with human-in-the-loop
Automated consistency, and traceability checks
Integrated data, and systems
Logged, explainable AI and human decisions
Faster submissions, and inspections
Proactive care, and system execution
Further questions?
How quickly will this reduce manual work for our teams?
Built for regulated operations
RakerOne is designed for environments where patient safety, data integrity, and regulatory defensibility are mandatory.
Every workflow operates under explicit rules, approvals, and human-in-the-loop checkpoints. AI actions are logged, decisions are explainable, and outputs are traceable, making inspections, audits, and internal reviews predictable instead of disruptive.
Works with health systems
RakerOne sits on top of your existing stack instead of replacing it.
It integrates with EHRs, QMS, RIM, LIMS, ERP, document repositories, and partner portals, coordinating work across validated systems without triggering large-scale revalidation.
That means faster deployment, lower risk, and workflows aligned with how healthcare and pharma organizations already operate.
Managed outcomes
RakerOne is delivered as a managed platform, not a set of AI tools your team has to assemble and maintain.
Our forward enablement team designs the workflows, configures governance, integrates systems, runs the platform, and tracks performance over time.
You measure success in time reclaimed for care and science, faster regulatory outcomes, lower error rates, and continuous audit readiness, not in tools deployed or prompts written.
