THIS ISN’T THEORY.
IT’S ALREADY WORKING.
PRODUCTION SCALE
75, 826 Medical Necessity Reports generated
2,785 Prior Authorizations processed
Operating across 39 states
Why cellarian is different
Cellarian:
Focuses on upstream documentation
Uses compliantly sourced clinical inputs
Bases logic on published guidelines and payer criteria
Generates patient-specific justification — not templates
Has been implemented across 40 states
Integrates into existing workflows
This is documentation built for reimbursement decisions — not just medical records.
What This Means for Laboratories
Fewer denials tied to documentation gaps
85% prior authorization first-pass approvals for lab (where implemented)
Reduced audit exposure
Compliant documentation generated at the time of service
Support for payer denials and late entry documentation requests
Less manual effort for physicians and billing teams
More predictable cash flow
Built for Complex Testing Environments
Cellarian supports documentation for:
Toxicology testing
Molecular diagnostics
Respiratory pathogen, COVID & Flu panels
UTI, STI, women’s health, and wound testing
The complexity is handled by the platform — not your team.
Other companies only tell you what’s missing. Cellarian actually creates it. Compliantly.
Built by physicians who lived the problem
Cellarian was built by clinicians, billers and healthcare administrators who saw appropriate testing denied for documentation reasons — not medical ones.
The platform was designed to be automated and remove bureaucracy without interfering with care.
CELLARIAN IS TRUSTED BY:
