Lynsey Carroll
Regulatory & Clinical Consultant
Lynsey Carroll is a Regulatory and Clinical Consultant at MDC Associates with over six years of experience in the in vitro diagnostics (IVD) industry. She holds a PhD in Molecular Genetics from the University of Glasgow and brings great expertise in global regulatory strategy, technical documentation, and submission planning. Lynsey has supported a wide range of diagnostic technologies across therapeutic areas from molecular diagnostics and companion diagnostics to infectious diseases and Oncology. She has hands-on experience in FDA submissions, IVDR compliance, and MDR/CE marking for medical devices. Driven by a strong passion for project management, she excels at guiding innovative healthcare solutions through complex regulatory pathways to achieve successful market access.
