Director, Regulatory Affairs at the Canadian subsidiary of Hill-Rom
Regulatory Affairs Advisor
Danna Zylka is a medical device industry professional with 20 years of experience in research, quality management and regulatory affairs. She is currently the Director, Regulatory Affairs at the Canadian subsidiary of Hill-Rom, a global medical technology company that specializes in the development of technologies for advancing mobility, wound care and prevention, patient monitoring and diagnostics, surgical safety and efficiency, and respiratory health. Danna has extensive expertise in US and Canadian regulatory requirements, global quality standards and the monitoring of manufacturing functions within the medical device industry.