AI for hospitals, health systems, and pharma — built where patient safety is the non-negotiable constraint.
Clinical AI, document processing, regulatory submissions, and governance frameworks designed for HIPAA, FDA AI/ML-SaMD guidance, and the EU AI Act's highest-risk classifications.
AI is reading scans, routing patients, and processing prior auths. Most of it is ungoverned.
AI in healthcare is no longer a future state. Clinical decision support tools are influencing diagnosis and treatment recommendations at hospitals across the country. Medical imaging AI is reading scans before the radiologist. Prior authorization systems are making coverage decisions affecting patient access to care. EHR documentation tools are generating clinical notes from ambient conversations.
The FDA has published guidance on AI and machine learning-based Software as a Medical Device. HIPAA applies to AI training data containing protected health information. The EU AI Act classifies AI used in medical diagnosis as high-risk — with the full compliance framework active. And the governance gap in most health systems is significant. The tools were deployed. The documentation was not created. The oversight was not designed in.
Five AI systems designed for the clinical and administrative environment.
Clinical AI Governance Framework
A complete governance infrastructure for clinical AI deployments — model inventory, pre-deployment documentation, bias testing across patient populations, human oversight design, and incident response planning. Built to satisfy FDA AI/ML-SaMD guidance and EU AI Act high-risk requirements.
RERIGHT service: AI Governance Audit + Governance PlaybookEHR and Clinical Document AI
Automated extraction, classification, and routing of clinical notes, lab results, discharge summaries, and prior authorization documents. AI that processes the administrative volume so clinical staff processes the exceptions. Full HIPAA-compliant data handling. Audit trail on every document action.
RERIGHT service: Fintech & Document AIPrior Authorization AI Pipeline
AI that classifies authorization requests, matches against coverage criteria, routes clear approvals automatically, and queues clinical edge cases for human review. Reduces average authorization time from days to hours. Reduces denial rates through better criteria matching.
RERIGHT service: Document AI + Agent OrchestrationClinical Knowledge RAG System
A RAG architecture built over clinical guidelines, formularies, policy documents, and institutional protocols — queryable by clinicians and administrative staff. Answers grounded in specific documents with citation attribution. Built for environments where an incorrect answer has clinical consequences.
RERIGHT service: RAG ImplementationRegulatory Submission Document AI (Pharma)
For pharmaceutical and life sciences organizations — AI that processes and organizes the document volume of regulatory submissions, safety signal reports, and clinical trial documentation. Designed for 21 CFR Part 11 compliance and FDA submission requirements.
RERIGHT service: Document AI + GovernanceThe regulations governing AI in healthcare.
HIPAA
Applies to any AI system trained on or processing protected health information. Data governance and access controls required.
FDA AI/ML-SaMD Guidance
Governs AI functioning as medical device software. Pre-market considerations, performance monitoring, change management requirements.
ONC Health IT
Interoperability and data access requirements affecting AI systems connected to EHR infrastructure.
EU AI Act
High-risk classification for AI used in medical diagnosis and treatment. Full compliance framework required.
21 CFR Part 11 (Pharma)
Electronic records and signatures requirements for AI systems in drug development and manufacturing.