Tuesday, June 13 from 10:30 – 11:15 a.m. EDT
Location: Room 3D05

• What is biocompatibility?
• How to classify a device and select endpoints for analysis
• Difference between horizontal and vertical standards and FDA guidance documents
• Common differences between ISO 10993-1 and FDA expectations
• Sample preparation for testing
• What standards are most commonly used for the evaluation of each endpoint
• Introduction to common biocompatibility methods

Speaker:

Patricia Curry, Ph.D.
Business Development Director, Labcorp

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