Virtual Program: Lifecycle Regulatory Compliance for Medical Devices

Leaders in industry, agencies and the legal profession share their expertise on the regulatory frameworks and industry best practices for compliant medical devices. Thomas C, Knott, senior regulatory consultant for KARA and Associates and FDA veteran, leads an interactive program that covers:

• FDA Inspections
• Imports and Exports
• Quality System Regulation—Design Control
• Changes in the 510(k) Process and Discussion of MDUFMA
• Registration and ListingQuality Systems—The Business Case for Quality