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:

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