Defensible IV Room Cleaning. Documented. Validated. Inspection-Ready.

Most facilities don’t fail inspections because they lack cleaning policies—they fail because they cannot prove execution, consistency, and competency.

Where Facilities Fail During Inspection

Recent State Board of Pharmacy and Joint Commission inspections continue to cite the same preventable failures—not due to lack of policy, but lack of execution and defensible documentation.

  • Inconsistent or undocumented IV room cleaning

  • Lack of sporicidal agent documentation and rotation

  • No verification that cleaning is performed correctly

  • EVS or pharmacy staff cleaning without competency validation

  • Logs completed after the fact and not inspection-defensible

Under USP <797> (2023) and TSBP Rule 291.133, facilities must demonstrate:

  • Cleaning is performed as required

  • Personnel are trained and competency validated

  • Documentation is complete, accurate, and retrievable during inspection

We Convert Cleaning Into a Defensible Compliance System

RigorRx provides independent, third-party validation of your IV room cleaning and disinfection program.

We do not replace your EVS or pharmacy staff.

We ensure:

  • Cleaning is performed correctly

  • Processes are standardized

  • Documentation is inspection-ready

  • Your facility can defend its practices under survey

Monthly On-Site Validation

  • Observation and verification of IV room cleaning

  • ISO-classified areas, PECs, and high-touch surfaces

  • Immediate correction of deficiencies

Sporicidal Compliance Oversight

Defensible Documentation

Process Standardization

  • Verification of EPA-registered sporicidal use

  • Frequency and rotation aligned with USP <797>

  • Elimination of common compliance gaps

  • Completed cleaning logs (not templates—executed records)

  • Timestamped validation records

  • Inspection-ready documentation systems

  • Alignment with USP <797> (2023)

  • Alignment with TSBP Rule 291.133

  • Integration with infection control expectations

How It Works

Step 1 — Assessment

Review current cleaning practices, logs, and products used

Step 2 — Validation

Observe or perform cleaning with real-time correction

Step 3 — Documentation

Generate defensible, inspection-ready records

Step 4 — Standardization

Implement repeatable processes aligned with USP <797>

Get Ahead of Your Next Inspection

Identify gaps before surveyors do. Strengthen your documentation. Reduce your risk.