On-Demand Webinar: Biological Indicator Incubation and Reduced Incubation Time

What You'll Learn in Our 45-Minute Webinar

✓ ISO 11138-7 and ISO 11138-8 Standards – Understand how these standards affect your BI selection, incubation protocols, and compliance requirements

✓ Delayed Cultivation Protocols – Learn how to establish justified time intervals when immediate post-sterilization incubation isn't possible

✓ Troubleshooting Unexpected Positives – Step-by-step investigation procedures including sub-culturing, organism identification, and root cause analysis

✓ Proper SCBI Interpretation – Distinguish actual growth from thermal degradation or chemical residuals; correct use of negative control units

✓ RIT Validation Requirements – Clarify what manufacturers must validate versus what end users need to verify

✓ Culture Condition Best Practices – Proper incubation temperatures, aseptic technique, and documentation requirements

This webinar is essential for:

• QA/QC Managers overseeing sterilization monitoring programs
• Sterile Processing Department Managers implementing BI protocols
• Validation Engineers developing or qualifying sterilization cycles
• Regulatory Compliance Officers ensuring FDA and ISO compliance
• Microbiology Lab Managers responsible for BI cultivation and interpretation
• Quality Engineers troubleshooting sterilization process issues

Industries served: Pharmaceutical manufacturing, medical device manufacturing, hospital sterile processing, compounding pharmacies, research laboratories