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Corporate Practice of Medicine Compliance

cpom-compliance

Drafts Corporate Practice of Medicine (CPOM) compliance structure documents for healthcare entities. Covers compliant organizational models (PC/PA, MSO, friendly PC), MSA architecture, operational compliance checklists, and state-specific regulatory analysis. Use when structuring healthcare opera...

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SKILL.md

Full skill instructions

Corporate Practice of Medicine Compliance

Drafts a regulatory compliance framework ensuring lawful separation of corporate ownership from medical practice under CPOM doctrine.

Prerequisites

Gather before drafting:

  1. Entity details — structure, state(s) of operation, healthcare sectors (medical, dental, optometry, telemedicine, PT)
  2. Existing agreements — MSA/​MSO arrangements, physician employment contracts, governance documents
  3. Jurisdictional scope — all states where entity operates or plans to expand
  4. Business model — revenue structure, physician compensation methodology, admin service arrangements

Document Structure

1. Introduction & Scope

  • Define CPOM doctrine and application to the entity
  • State jurisdictions covered
  • Identify violation consequences: license revocation, contract voidability, criminal prosecution, civil fines

2. State-Specific CPOM Analysis

Produce a jurisdictional matrix covering: state, prohibition level (strict/​moderate/​permissive), key statute, exemptions, enforcement pattern.

  • Limit to entity's actual operational footprint — no generic 50-state surveys unless requested
  • Note sector-specific variations (telemedicine, dental, optometry, PT face different scrutiny)
  • Flag recent legislative changes
  • Mark uncertain citations with [VERIFY]

3. Compliant Organizational Structures

Compare models:

StructurePhysician ControlRiskBest For
PC/​PAFull ownership + governanceLowSingle-state practices
MSO + PCPC controls all clinical decisionsLow-MedMulti-state platforms
Friendly PCNominal — high regulatory scrutinyHighAvoid unless carefully structured
PPMShared governanceMediumLarge physician groups

For each: governance requirements, operational boundaries, de facto control scrutiny factors, selection criteria.

Friendly PC warning: Never present as low-risk. Always flag for heightened scrutiny.

4. Management Services Agreement (MSA) Architecture

MSO-permissible: billing, collections, revenue cycle, non-physician HR, facility management, IT, marketing, financial reporting.

Reserved to physician entity (non-delegable):

  • Clinical decision-making and patient care protocols
  • Physician hiring, credentialing, supervision, termination
  • Fee-setting for medical services
  • Patient acceptance, treatment, referral, discharge
  • Quality standards and peer review

Required MSA provisions: FMV compensation (no clinical-outcome incentives), physician exit rights, physician final authority on clinical matters, mutual CPOM compliance obligations, FMV documentation defensible under AKS/​Stark, independent audit rights.

5. Operational Compliance Checklist

Cover these control points with responsible party and frequency:

  • Physician hiring/​credentialing — PC makes all final decisions
  • Clinical protocols — developed by physicians without MSO interference
  • Fee setting — PC independently determines charges
  • Patient care decisions — no MSO influence on acceptance, treatment, referral, discharge
  • Marketing — accurately represents physician-owned nature of practice
  • Board minutes — separate PC and MSO minutes documenting independent decision-making
  • Approval workflows — clear audit trail showing physician authority

6. Training, Monitoring & Enforcement

  • Training: physicians, admin staff, executives — governance responsibilities, authority boundaries, legal risks (onboarding + annual)
  • Monitoring: quarterly MSA audits, annual decision-making review, annual FMV assessment, anonymous reporting channel (whistleblower-protected)
  • Enforcement escalation: corrective action plan → structural modification → relationship termination

7. Risk Assessment & Mitigation

Address: regulatory penalties, contract voidability, qui tam/​FCA exposure, reputational harm, discovery of violations.

Include self-disclosure decision framework: weigh severity, duration, patient harm, cooperation credit, jurisdiction-specific voluntary disclosure programs.

8. Conclusion & Authorization

  • Reaffirm ongoing compliance obligation with annual review
  • Review triggers: operational changes, new jurisdictions, legislative updates, enforcement actions
  • Signature blocks: business entity rep, physician entity leadership, legal counsel, effective date + next review

Critical Checks

  • All citations must be verified for current validity; mark uncertain with [VERIFY]
  • Address federal overlay (AKS, Stark Law, OIG guidance) alongside state CPOM — never analyze CPOM in isolation
  • Friendly PC arrangements always flagged for heightened scrutiny
  • Structure document for dual audience: legal/​regulatory reviewers and operational implementers
  • Reference OIG compliance program guidance and MGMA best practices where applicable

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