Head of Pre-Market Approval of Medical Device
Anvisa - Brazil
Karen Noffs
- Specialist in Health Regulation and Surveillance.
- Experience as a manager of the Ports, Airports and Borders department, responsible for licensing the import of products subject to health regulations.
- Experience as a manager of the department responsible for audits in medical device manufacturing industries, issuing the Good Manufacturing Practices Certificate - GMP.
- She currently holds the position of Head of Pre-Market Approval of Medical Devices
Brazilian Health Regulatory Agency
ANVISA - Brazil
Breaking Barriers: The Power of Regulatory Reliance
Thursday, April 24, 2025
8:15 AM – 9:30 AM East Coast USA Time