Diana is a highly accomplished Regulatory Affairs Expert with an MBA and a decade of experience navigating the complexities of global product life-cycle management. She possesses a remarkable ability to bridge regulatory needs with business goals, consistently ensuring market success. Her expertise spans strategic planning, global submissions (including EU, LATAM, APEC, and beyond), change management, and CMC dossier excellence. A skilled leader in CMC change management, she ensures smooth transitions and compliance. She is passionate about optimizing regulatory processes and is known for her collaborative approach, delivering exceptional results across teams.

Prior to focusing on regulatory strategy at Eliquent Life Sciences, Diana served in key roles in pharmaceutical companies, leading regulatory teams and coordinating product dossiers for EU and non-EU submissions. Her passion for optimizing regulatory processes, building strong relationships with health authorities, and driving successful outcomes makes her a trusted partner for organizations navigating the global regulatory landscape.