Audit Firm Design Partners

Bring one reviewer workflow we can validate together.

Share organization-level information about your current SNF or post-acute review process. The first conversation requires no client data. Do not include patient, client-confidential, engagement-confidential, or protected health information.

No PHI or client-confidential data. Do not enter patient names, DOBs, MRNs, chart text, facility-client names, active audit details, payer letters, or confidential engagement information. The current design-partner workflow uses SMEG-supplied synthetic information only.

Audit / Consulting Organization

Contact Name

Your Role

Approximate Reviewer Team Size

Primary Review Focus

Current First-Pass Workflow

Work Email

Phone

What part of the reviewer workflow takes the most time?

What would make a bounded paid synthetic calibration useful?

I confirm that this request contains no PHI, patient data, client-confidential data, active audit details, or chart text.

Review partner overview

This form prepares an email from your device; it does not upload data to SMEG. If your email app does not open, send organization-level details to smeg@suprememedicalevaluationgroup.com.

Best design-partner fit

A real reviewer team with a repeatable workflow.

• Reviews SNF or post-acute documentation
• Uses human clinical or audit reviewers
• Can begin with SMEG-supplied synthetic information only
• Will measure agreement, overrides, QA, time, and report usefulness
• Accepts that reviewers retain final authority

The boundary

SMEG assists first-pass documentation-risk review. It does not determine medical necessity, certify compliance, approve billing, provide legal advice, or guarantee payer or denial outcomes.

Before production data

BAA, security review, authorization, role access, audit logging, retention, deletion, hosting, and secure intake must be approved before production PHI is accepted.