Eric Henry

Sr. Quality Systems & Compliance Advisor
FDA & Life Sciences Practice, King & Spalding
 

Eric Henry, Senior Quality Systems and Compliance Advisor of FDA & Life Sciences Practice at King & Spalding law firm, is a veteran of the industry of more than 33 years. Since 2018, he has provided advisory and consulting services focused on regulatory compliance, enforcement and policy matters for industries regulated by the FDA. Henry delivers topnotch guidance on FDA requirements to professionals in medical device manufacturing, including but not limited to quality systems requirements, inspection preparedness and post-market obligations. He also advises corporate management and boards on their responsibilities and expectations of the FDA.

 

Sessions: 

Cybersecurity: The Current Regulatory Landscape and How to Defend Your Practices During an Inspection
The Impact of AI and New Technology on Regulatory Compliance
FDA’s Shift from QSR to ISO 13485:2016: A Significant Change for Inspections
Validating Your Systems and Equipment for Compliance