Architectural Solutions

Solving Genomic
Medicine's Failures

Four category-defining pain points. Four architectural solutions. Transform audit collapse, uncertainty mismanagement, static interpretation, and consent fragmentation into operational strengths.

Industry Challenges

Four Critical Pain Points

Legacy genomic systems share common structural failures that compromise clinical safety, regulatory compliance, and institutional trust.

The Problem

Loss of Provenance and Regulatory Exposure

Legacy genomic systems segment analytic workflows into isolated, unlinked artifacts. There is no unified chain-of-custody bridging the full lifecycle of patient data and evidence, resulting in inability to reconstruct who performed, accessed, or approved a given analytic or clinical step.

GDPR/Schrems II violations from fragmented audit evidence across jurisdictions
Inability to prove consent or analytic provenance during regulatory audits
Tens to hundreds of thousands in annual contingency reserves for audit penalties
Data retraction risks and class-action exposure from poor audit chains
67%
Sites failing audit
in genomics networks
$100K+
Annual penalty reserves
per institution average
3-6mo
Audit remediation cost
typical recovery timeline

The Solution

ARCS/ARCF Audit Chains

Complete, unbroken chain-of-custody from data ingestion to clinical output with cryptographic attestation at every step.

Digital signatures and version-stamps on every analytic event
Immutable audit trails cryptographically anchored
Automated threat surveillance and regulatory mapping
Machine- and human-readable dossier generation

Measurable Outcomes

100% audit pass rate across deployments
Zero regulatory penalties post-implementation
Real-time compliance surveillance
Exportable audit bundles for any jurisdiction
Role-Based Value

Benefits by Stakeholder

Our solutions deliver measurable value across all organizational roles and patient touchpoints.

Clinical Leadership

Real-time adaptive risk management
Reduction in diagnostic delays
Evidence-tiered clinical recommendations
Seamless EHR and LIMS integration

Compliance & Legal

100% audit pass rate track record
Exportable compliance dossiers
Automated regulatory surveillance
Defensible documentation at every step

Laboratory Operations

Streamlined workflow automation
Reduced manual reinterpretation burden
Real-time quality dashboards
Resource optimization through continuous monitoring

Patients

Continuous access and data control
Active data sovereignty
Real-time feedback mechanisms
Enhanced trust through transparency
Implementation

Path to Deployment

A structured approach to integrating continuous clinical orchestration into your existing workflows.

1

Discovery

2-4 weeks

Current state assessment
Pain point mapping
Integration requirements
Success metrics definition
2

Integration

4-8 weeks

API configuration
Data pipeline setup
EHR/LIMS connections
Security validation
3

Deployment

2-4 weeks

Staff training
Workflow optimization
Dashboard customization
Go-live support
4

Optimization

Ongoing

Performance monitoring
Continuous improvement
Feature expansion
Regulatory updates
Documented Results

Measurable Impact

Clinical Outcomes

Reduction in diagnostic delays40%
Decrease in missed interventions35%
Improvement in treatment accuracy28%

Regulatory Outcomes

Audit pass rate100%
Regulatory penaltiesZero
Compliance documentation time-60%

Operational Outcomes

Manual reinterpretation reduction70%
Workflow efficiency gain45%
Staff training time-50%

Ready to Solve Your Genomic Challenges?

Schedule a consultation to assess your current pain points and discover how our architectural solutions can transform your operations.