Your Lab Did the Work.

Why Aren’t You Getting Paid?


You already know the problem.

The question is whether it's worth doing something about it.

[COMPANY NAME] partnered with Cellarian to help laboratories address documentation-related reimbursement challenges without adding new software, new logins, or new provider workflows.

200,000+

Reports Generated

Payer aligned and patient-specific

39

US States Covered

Supporting labs and RCM partners nationwide

80-90%

First Pass Prior Auth Success

Client reported

SUCCESS

Successfully Used

in TPE (Targeted Probe and Educate) & IRO (Independent Review Organization) Audits

Most laboratories already understand that documentation impacts reimbursement.

What stops them from acting is the assumption that solving the problem will create more work.

Cellarian was designed to do the opposite.

·       No provider workflow changes

·       No new software installation

·       No separate login

·       Works within the existing workflow

The Cellarian Solution workflow infographic

Most solutions fix denials after they happen. Cellarian prevents them before they occur.

The Cellarian Solution is Simple, Reliable, and Works

The Cellarian Solution workflow infographic

Set it up once, then it works on autopilot.

No portal switching. No reconstruction after denial. No added documentation burden for lab staff.

Does it work? In a word, YES.

One Cellarian client improved toxicology prior authorization approval rates from under 10% to more than 60%. Cellarian-generated documentation has also been used successfully in TPE audits and Independent Review Organization audits.

Revenue at Risk Assessment

How much earned reimbursement could be affected by documentation-related denials, records requests, prior authorization challenges, and audit activity?

Estimated Monthly Revenue at Risk

$0

Estimated Annual Revenue at Risk

$0

This is not a guarantee of recovery. It is a directional estimate of reimbursement potentially exposed to documentation-related friction.

Talk to Cellarian about protecting revenue

BUILT FOR HOW PAYERS ACTUALLY REVIEW CLAIMS

Why Cellarian is Different

Patient-Specific. Not Templated.

Every document reflects the provider’s clinical assessment of their patient.

Proprietary Documentation Engine. Not AI Hallucinations.

Built over years by experienced physicians, compliance specialists, and revenue cycle experts.

Always Up To Date.

The Cellarian Engine is continuously refined to meet ever-changing payer requirements.

Built for the realities of toxicology and molecular testing:

Physician-Owned Labs

Support documentation consistency while reducing provider burden and audit exposure.

Clinical Reference Labs

Scale documentation workflows across multiple payer environments and referring providers.

Hospital Labs and Health Systems

Standardize documentation across departments and ordering environments.

Substance Use Treatment Providers

Support testing workflows operating under heightened payer scrutiny.

Pain Management Practices

Generate documentation aligned with testing frequency, medical necessity, and payer expectations.

Stronger Documentation.

Stronger Revenue Cycle.

See how Cellarian can help your lab reduce denials, accelerate reimbursement, and stay audit-ready.

Operational scale. Real-world usage

  • 148,000+ medical necessity reports generated

  • 52,000+ prior authorizations generated

  • Operating across 39 states

  • 80–90% first-pass prior authorization success (client reported)

  • Supports toxicology, molecular, and PGX workflows