How to design an Instruction For Use and validations for EU and US
In this free on-demand webinar, Kathleen Peymen, PhD, Senior Expert, takes you on an road trip to discover...
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Biocompatibility as a Critical Design Input
For any medical device contacting a patient, a biocompatibility evaluation is required before the device can be...
Disinfectant Efficacy Testing on Site Specific Surfaces
Disinfection efficacy studies play a significant role in the Pharmaceutical manufacturing environment in ensuring that the surfaces...
What’s New with Reprocessing Validations for Reusable Medical Devices?
There have been many great strides surrounding the guidance for reprocessing (cleaning, disinfection, and/or sterilization) validations for...
Advancing Microbial-Contamination Detection Through Rapid Sterility Testing
Increasing industry and product demand for expedited product release reinforces the need to embrace rapid sterility technologies....
Single Use Endoscopes Critical Safety and Regulatoy Considerations for Manufacturers
The transmission of infections via endoscopy remains a critical concern due to the inherent design challenges of...
Implementing Parametric Release for EO Sterilization
Join us for an informative webinar that reviews the benefits of parametric release and how to establish...
The Impact of Sterilization Modality on Connected Devices with Electronic Components
devices. The complex nature of connected devices, which often involve a combination of materials and electronic components, can...
The Transfer of Medical Device and Pharmaceutical Products between Radiation Sterilization Modalities
With the growing demand for sterilization of medical devices and pharmaceutical products, the industry is increasingly looking...
Container Closure Integrity Testing for Pharmaceutical Sterile Barrier Packaging
Container Closure Integrity Testing (CCIT) is crucial for evaluating the sterile barrier integrity of pharmaceutical packaging, including...