Marta Stepien

Vice President of Clinical, Regulatory, and Quality Affairs at Sleepiz AG, Zürich

WHO AM I 

Marta possesses a strong academic background and experience in biology, neuroscience, and clinical research. She obtained her Bachelor’s degree in Medical Biotechnology from the Medical University of Lodz and pursued a Master’s in Biology, specializing in Neuroscience, at ETH Zürich. Throughout her time in academia, Marta has contributed  to research on neurofeedback and brain stimulation technologies for stroke rehabilitation at the Neural Control of Movement Lab in Zürich. Marta’s international experience includes several research internships in Latin America and Asia where she explored practical applications of different biology branches. She currently holds the position of Vice President of Clinical, Regulatory, and Quality Affairs at Sleepiz AG, Zürich. Here, she is responsible for formulating global regulatory strategies, leading audits, and managing international projects. One of her notable achievements was the efficient introduction of a novel medical device to the EU market by securing the certification under EU Medical Device Regulation. Marta brings expertise in regulatory affairs (MDR, FDA),  compliance (ISO, GDPR, HIPAA), and interdisciplinary medical device knowledge (software, active medical devices, sleep and cardiorespiratory disorders) to her career.