Start with the work that is constrained now.
StromaOS solutions are organized around pharmaceutical evidence operations, not generic AI use cases. Each solution combines domain context, reusable skills, governed agents, quality gates, human authority, and end-to-end evidence traceability.
Governed execution across the pharmaceutical lifecycle.
Each solution has its own operating model, evidence context, intelligence modules, workflow patterns, quality controls, human authorities, and measurable outcomes.
Connect scientific evidence to target and portfolio decisions.
Target mechanism intelligence, translational evidence, preclinical risk, and portfolio strategy with preserved assumptions, uncertainty, and decision rationale.
Explore Discovery & Portfolio →Run clinical evidence work as one coordinated system.
Protocol, study, site, patient, endpoint, operations, MIDD, safety, and real-world evidence connected through governed execution.
Explore Clinical Development →Preserve the chain from incoming evidence to safety action.
Case evidence, signals, aggregate analysis, medical assessment, escalation, regulatory action, and lifecycle follow-up in one traceable chain.
Explore Safety & Pharmacovigilance →Build regulatory output from governed evidence.
Connect strategy, claims, source evidence, analyses, authoring, review, commitments, approvals, and submission-ready content.
Explore Regulatory & Submission →Clear the request queue without adding headcount.
Feasibility, governed cohort creation, scenario comparison and expert approval, with approved populations reused across HEOR, safety, medical writing and clinical development.
Explore Real-World Evidence & Epidemiology →Carry evidence from development into value demonstration.
Evidence planning, economic analysis, value dossiers, payer questions, HTA response, local adaptation, and market learning.
Explore HEOR & Market Access →Keep scientific response connected to approved evidence.
Scientific monitoring, field insight, medical information, communications, review, response, and reuse inside approved boundaries.
Explore Medical Affairs & Information →Connect quality evidence, investigations, change, and regulatory impact.
Deviations, trends, CAPA, process knowledge, suppliers, stability, change control, filings, commitments, and effectiveness.
Explore CMC Quality →Govern the work that sits between functional systems.
Knowledge management, evidence generation planning, portfolio reviews, governance, decision packages, and lifecycle handoffs.
Explore Cross-Functional Operations →Every solution is built on the same governed execution pattern.
StromaOS does not create a new silo for each function. Each solution uses the Shared Semantic Data Layer, Governance Spine, execution environment, evidence record, and organizational memory while preserving the distinct authority and standards of the function.
Explore the platformTwo capabilities span every solution.
Knowledge Management and Evidence Generation Planning are not standalone repositories. They are cross-cutting operating capabilities that preserve what the organization knows, what evidence it needs, what work is committed, and how decisions evolve.
Scientific memory, evidence context, definitions, decisions, assumptions, qualified outputs, lessons, and reusable organizational knowledge.
Explore Knowledge Management → Evidence Generation PlanningEvidence questions, gaps, studies, analyses, commitments, markets, milestones, dependencies, owners, and decision readiness.
Explore Evidence Generation Planning →Start with one evidence operation that is visibly constrained.
Connect the sources and specialist tools already in use. Define the evidence standard, authority, quality gates, and human decisions. Then run the work as a governed system and expand from the shared context.