Bio
A Veterinary Medicine graduate at the Warsaw University of Life Sciences. Associated with Clinical Trials since 2 years, previously worked with Medicinal Products. Responsible for designing and scientifically coordinating performance studies conducted in accordance with ICH-GCP principles and the requirements of IVDR Regulation 2017/746, ISO 20916:2019, FDA or other regulatory bodies. She participates in the development of study protocols, informed consents forms, investigator brochures and other research materials for clinical projects related to the testing of in vitro diagnostic medical devices.