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  • Feature Story

RECORDED WEBINAR: Strategy for Biological Safety Evaluation of Medical Devices

February 12, 2018

Biological safety evaluation of medical devices is a part of regulatory requirement. The scope of the webinar is to understand the strategy behind the biocompatibility testing and a step wise approach to implement biocompatibility requirements. The topics covered are as follows:

    • Biocompatibility strategy
    • Role of material characterization
    • Biocompatibility studies and Toxicology risk assessment

 

Register to view the recording: http://connect.ul.com/HSWBML180118BIOCOMP_LP-On-Demand.html

Your Speaker: S Haribabu, Project Engineer – Medical Device Testing, UL

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