Sarah Johns

Sarah Johns is the Associate Director of Regulatory Affairs at MCRA, bringing over 10 years of regulatory affairs experience in IVD medical devices, particularly in Companion Diagnostics. Previously, Sarah held several roles at QIAGEN, including Regulatory Affairs Specialist and Senior Manager Regulatory Affairs. Sarah is skilled in various FDA submission types, including IDE, CBE, PMA, and pre-submissions, as well as CE marking and IVDR requirements. They earned a Bachelor of Science in Human/Medical Genetics from the University of Leeds.