Tatiana is a pharmacist with a degree from the State University of Londrina (UEL), specialising in Clinical Analysis and a postgraduate degree in Industrial Toxicology (ongoing). Throughout her career, she has accumulated extensive experience in regulatory submissions for various markets, including FDA (510(k)), CE Marking under MDR 2017/745, and ANVISA. She also has extensive experience in the preparation and review of technical documentation, risk management, biological assessment, quality management systems, and compliance strategies with international standards.