Previously Recorded On February 23, 2022
Change Management, especially related to a medical device’s design, is one of the most commonly-cited issues in FDA 483s and Warning Letters. Unfortunately, change is constant in the medical device industry, so it’s imperative to learn how to effectively evaluate change and incorporate findings into biocompatibility testing and documentation. In this webinar, industry expert Thor Rollins from Nelson Labs will teach you how to:
Thor Rollins | Nelson Labs