📢 Invitation to the SPARK Studio workshop | Biomarker to CE/UKCA-marked IVD test – the regulatory journey | SPARK The Midlands | Erica Conway

Dr. Erica Conway has over 20 years of experience in regulatory affairs and quality assurance, primarily in the In Vitro Diagnostic (IVD) medical device field. She joined MCRA in August 2022 as VP of IVD Regulatory Affairs. Before MCRA, Erica worked in pharmaceutical regulation and clinical trials, moved into IVD medical devices in 2006, and later served as Global Head of IVDs and Head of IVD Notified Body at the British Standard Institution (BSI). At BSI, she played a key role in implementing the IVD Regulation (IVDR, (EU) 2017/246) and the successful designations of both the UK and the Netherlands organizations to the IVDR.