🔧 Detailed Service Scope

1️⃣ Autoclave Cycle Verification

Technical evaluation of sterilization cycles:

• Temperature verification (121°C / 134°C cycles as applicable)

• Pressure monitoring review

• Exposure time validation

• Load configuration review

• Steam penetration assessment

• Alarm & safety system check

Ensures proper sterilization parameters are achieved.

2️⃣ Sterilization Logbook Audit

Documentation compliance review:

• Cycle recording format verification

• Batch record validation

• Operator signature review

• Parameter entry accuracy check

• Logbook retention practice review

Improves audit readiness.

3️⃣ Biological Indicator Test Coordination

Validation of sterilization effectiveness:

• Biological indicator placement guidance

• Test cycle coordination

• Spore strip validation support

• Incubation result documentation guidance

• Failure investigation support

Confirms actual microbial destruction effectiveness.

4️⃣ Waste Pre-Treatment SOP Review

Evaluation of pre-autoclaving practices:

• Waste segregation before sterilization

• Bag sealing method review

• Container loading pattern guidance

• Moisture content check

• Chemical disinfectant pre-treatment review (if applicable)

Reduces sterilization failure risk.

5️⃣ Sterility Confirmation Documentation

Structured documentation support:

• Sterilization confirmation report format

• Batch validation checklist

• Deviation documentation guidance

• Corrective action record support

• Compliance file organization

Ensures inspection-ready documentation.

📦 Deliverables

• Autoclave cycle verification report

• Logbook audit checklist

• Biological indicator test documentation support

• SOP improvement recommendation report

• Sterilization validation summary

• Compliance readiness report

🎯 Key Benefits

✔ Verified sterilization effectiveness
✔ Reduced contamination risk
✔ Improved regulatory compliance
✔ Audit-ready documentation
✔ Safer waste disposal process