Radiation Microbiology in Pharmaceutical Products
Microbiological testing on pharmaceutical products can sometimes be confusing, especially when dealing with sterilized components or a...
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Beyond LAL: The Future of Endotoxin Testing Is Recombinant
Bacterial endotoxins can negatively impact the quality and effectiveness of pharmaceutical products, medical devices, and other materials....
Reprocessing Implants: Challenges for Validation
Implant caddies or similar implant storage units for single use implants are commonly opened and exposed during...
End-to-End Human Factors for Medical Devices and Reprocessing Usability Testing
Human factors engineering is essential to designing medical devices and healthcare products that are safe, intuitive, and...
Unmasking the Unknown: How Mass Spectrometry Delivers Accurate Identifications
In this webinar, presented by our Senior Expert LC/MS, Ruud Cuyvers, you’ll expand your knowledge on unexpected impurities in Drug...
Disinfectant Efficacy Testing on Site Specific Surfaces
Disinfection efficacy studies play a significant role in the Pharmaceutical manufacturing environment in ensuring that the surfaces...
Materials & Packaging for Terminally Sterilized Medical Devices
Join us for an insightful session that covers the essential aspects of packaging, focusing on both basic...
Reprocessing Validations Flexible Endoscopes and AAMI ST91
The newly revised AAMI ST91:2021 standard provides comprehensive guidelines for the processing of flexible and semi-rigid endoscopes...
Testing Disinfectant Agents for Antimicrobial Action on Hard Surfaces
Qualifying disinfectants on surfaces within a pharmacopeial manufacturing environment is a crucial step before they can be...
Design Control for the Contract Research Organization
Design Control is a fundamental requirement set forth by the FDA, detailed in 21 CFR 820. It...