Business insights and articles written by our team of world-class professionals
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.
As of March 7, 2024, LexaMed is actively recruiting for the following positions: Microbiologist, Lab technician, and Chemist.
LexaMed’s ISO 17025 Accreditation Certificate has been updated on our Company Document page. You may also download a copy of it here.
LexaMed’s DEA Controlled Substance Registration Certificate has been updated on our Company Document page. You may also download a copy of it here.