Dorit Pessler-Cohen is a highly experienced specialist in regulatory affairs with a Ph.D. in Biology. With significant knowledge and experience in pharmaceutical regulation of FDA, EMA, and other regulatory authorities, Pessler-Cohen is well versed in medical device FDA high standards (PMA) and has extensive experience in developing in-vitro diagnosis tests. Having worked with regulatory guidelines for drugs and medical devices, Pessler-Cohen is also experienced in team management and project management. She brings a unique professional perspective to the regulatory affairs field with her skillset and an eagerness to learn.