News

News

News

Ask An Expert: FAQ’s About Microbiological Testing for Medical Devices and Pharmaceuticals

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 ...
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Sterilization Process Validation

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 ...
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Cleaning Validation for Reusable Medical Devices

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, ...
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LexaMed Turnaround Times

LexaMed . Lot Release Testing Turnaround Times Published:  February 18, 2025 Author:  Hayden Rowan Topics:  Medical Device Testing, Pharmaceutical Testing, Lot Release Testing, Turnaround Times ...
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MSS Study of Reconstituted or Diluted Drugs

Microbial Stability Study of . Drug Products Published:  February 7, 2025 Author:  Anne M. Schuler Topics:  Microbial stability studies, pharmaceuticals, reconstituted drug products, diluted drug ...
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Updated ISO 13485-2016 Certificate

LexaMed’s ISO 13485-2016 Certificate has been updated on our Company Document page.  You may also download a copy of it here.
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