Priscila Sanada has over 13 years of Regulatory Affairs experience and is a valuable member of the consulting team of Emergo by UL in Brazil. She works on medical device consulting projects for all risk classes. Priscila's regulatory background includes Brazil and Mexico registrations, MDR regulations, global regulatory strategy advising, and regulatory research on markets in Latin America. In her current role, Priscila oversees Emergo by UL's Senior Regulatory Affairs Consultants in Brazil and has peer reviewed more than 100 regulatory filings and reports.