Mrs Ana Quinn

After obtaining a degree in Biomedical Sciences and a Master’s in Clinical Microbiology, Ana dedicated her career to regulatory and clinical affairs. 

With over a decade of experience in the medical device industry, she has collaborated with manufacturers globally, supporting them with compliance with MDR and FDA requirements and authoring more than 250 deliverables for Class I to III devices.

• Advanced
• Audit/Inspection
• Compliance
• Product Lifecycle
• Regulatory Intelligence/Policy
• Regulatory writing/documentation
• Risk management
• Europe
• Global
• United States
• Diagnostics/IVDs
• Medical Devices