OIG Investigation Procedures / Consensual Non-Telephone Monitoring / Authorization in Non-Sensitive Cases

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Note:  The following article synopsis was NOT provided by HCPro. It was created by Find-A-Code/innoviHealth.

Article Overview

This premium article explains the administrative and approval process for consensual non-telephone monitoring in OIG investigation procedures. It is aimed at compliance, investigative, and legal personnel who need to understand the categories of information required in an authorization request, the roles of headquarters and Justice Department personnel, and the need for written consent documentation. The article focuses on non-sensitive cases and covers the general elements that must be included in the request package without providing broader policy background.

Why This Topic Matters

Understanding the required approval framework helps investigators and compliance staff prepare complete monitoring requests and maintain proper documentation for oversight and audit purposes.

What You Will Learn

  • The general approval workflow for consensual monitoring requests
  • The categories of information that must be included in a monitoring authorization memo
  • Which officials and attorneys are involved in review and approval
  • The documentation expected from consenting parties
  • The timing and duration topics addressed in authorization requests

Who Should Read This

  • OIG investigators
  • Compliance professionals
  • Government attorneys
  • Healthcare compliance staff
  • Audit and oversight personnel

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