Bio
Graduate of Laboratory Medicine at the Medical University of Lodz and Clinical Research and Biomedical Research at the Medical University of Poznan with two years of experience in clinical research.
She is responsible for monitoring clinical trials in accordance with ICH-GCP guidelines, ISO 20916:2019, Standard Operating Procedures and all applicable regulations. Serves as an intermediary between the sponsor and the site, providing support throughout the research process. Performs monitoring visits and training on the study. Verifies the quality of the data obtained and the compliance of the procedures performed with the study protocol.