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Bioburden Monitoring ISO 13485 §7.5.2 & 7.5.7 (Executive Series #88)
Dose Audits ISO 13485 § 7.5.2 & 7.5.7 (Executive Series #89)
Biological Indicators ISO 13485 § 7.5.2 & 7.5.6 (Executive Series #90)
Sterility Assurance Level (SAL) ISO § 7.5.2 & 7.5.7 (Executive Series #94)
Sterilization Overkill Methods ISO 13485 § 7.5.6 & 7.5.7 (Executive Series #93)
Sterilization Revalidation – ISO § 7.5.6 and 7.5.7 (Executive Series #95)
Identification 820.60 & ISO 13485 § 7.5.8 (Executive Series #29)
Aseptic Processing ISO 13485 § 6.3 & 7.5.2 (Executive Series #87)
Medical Device Sterilization Validation ISO § 7.5.6, 7.5.7, & 820.75 (Executive Series #81)
Appropriate uses for Product Sterility Testing – when is sterility testing appropriate
Contamination Control and Sterility Assurance for Compounding Facilities
Technical Tuesday: Bacterial Endotoxin Testing in 2022 - Is My Laboratory Conducting It Right?