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ON-DEMAND WEBINAR

ON-DEMAND WEBINAR

Handling Unexpected Biocompatibility Test Results in Medical Device Development

Published Date: July 19, 2024

Getting unexpected or failing test results for any biocompatibility test can feel like the end of the line for a medical device. As a vital step in device development, biocompatibility testing has a major effect on the approval process timeline. This 10-minute presentation sheds light on the bleak consequences of unexpected biocompatibility test results. It outlines several questions designers should ask as well as answer throughout an investigation to understand the results and what they mean for patient safety and regulatory compliance.

Learn more about the presenter below.

Audrey Turley

Audrey Turley

RM (NRCM), CBA (ASQ)
Director of Expert Advisory Services & Biocompatibility Expert

Audrey Turley has over 25 years of experience working in research, laboratory, and test design functions in the medical device industry. She is a biocompatibility expert, having performed all the in vitro tests offered at Nelson Labs, which include cytotoxicity (MEM and agar overlay), hemolysis (PTT, PT, complement activation, blood circulation, ASTM, and NIH methods),...

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