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Master Challenge Devices and Process Challenge Devices in Sterilization Validation Published: May 18, 2026 Author: Hayden B. Rowan Topics: Master Challenge Devices, Process Challenge Devices,
Use of Biological Indicators in Sterilization Validations . Published: February 11, 2026 Author: Jim G. Whitcomb Topics: Biological Indicators, Sterilization Modalities, Validation Requirements, Sterility Assurance
LexaMed’s ISO 17025 Accreditation Certificate has been updated on our Company Document page. You may also download a copy of it here.
Ask An Expert: Your Routine Microbiological Testing FAQ’s Answered Published: May 29, 2025 Author: Anne M. Schuler Topics: Method Validation, Bioburden Analysis, Sterility Testing, Endotoxin
Sterilization Process Validation Published: April 7, 2025 Author: Jim G. Whitcomb Topics: Sterility Assurance Level, Ethylene Oxide (EO), Gamma, E-Beam, Steam, Bioburden Determinations, Protocol Report
Cleaning Validation for Reusable Medical Devices Published: March 20, 2025 Author: Anne M. Schuler Topics: reusable medical devices, cleaning validations, reprocessing of reusable medical devices,
LexaMed . Lot Release Testing Turnaround Times Published: February 18, 2025 Author: Hayden Rowan Topics: Medical Device Testing, Pharmaceutical Testing, Lot Release Testing, Turnaround Times
Microbial Stability Study of . Drug Products Published: February 7, 2025 Author: Anne M. Schuler Topics: Microbial stability studies, pharmaceuticals, reconstituted drug products, diluted drug
LexaMed’s ISO 13485-2016 Certificate has been updated on our Company Document page. You may also download a copy of it here.