is Senior Executive with Irish Medtech since May 2022 leading the regulatory affairs workstreams including the QA/RA forums and the Task Forces. Prior to joining IMA, she held senior positions in Telecommunications Industry Ireland and Audiovisual Ireland within Ibec overseeing the regulatory affairs and public policy work streams. She represented industry on the Government’s Task Force on Mobile Phone and Broadband. She continues to lead the 5G work stream within Ibec. Emer is an active member of Medtech Europe’s MD and IVD Regulatory Affairs Committee. She holds a first-class honours degree in electronic engineering and a PhD in the same discipline from University College Dublin.
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I’ve spent 20 years building companies in EdTech, MedTech, and consultancy, with the last 15 focused on AI and machine learning. My career has taken me from Singapore to Spain and Germany to Ireland, showing me how the right technology can transform organizations and outcomes.
As Head of Innovation at Trinzo, I help life science companies make AI practical — whether that means training teams, redesigning processes, or driving system change.
Before Trinzo, I was COO at Adaptemy, where we used machine learning to personalize learning for students, teachers, and ministries of education, and VP of Operations at WHYZE Health, leading AI projects that matched patients with the care they need.
With an MBA from Trinity College Dublin and further studies in AI (MIT), Blockchain (Oxford Saïd), and Digital Business (UCD), I bring a mix of education, technology, and innovation to every project — making AI accessible and impactful.
Hashan Dias is the Training Team Manager for Artificial Intelligence at BSI Group, where he leads global learning strategies to support AI operations and regulatory compliance. With over a decade of experience spanning medical devices, regulatory frameworks, and training leadership, he has designed and delivered impactful learning programs worldwide. A member of the UK national standards committee for IEC 60601-1, Hashan combines technical expertise with a passion for developing talent, driving culture transformation, and advancing excellence in AI and healthcare technology.
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Susan McMonagle is the Associate Director of Regulatory Affairs at Boston Scientific, bringing over 20 years of leadership in quality and regulatory roles across both start-ups and multinational medical device manufacturers. She currently leads a global team with responsibility for the regulatory strategy and compliance of devices including peripheral balloons, stents, and combination technologies.
With a MSc in Software Development, Susan combines regulatory expertise with technical knowledge, enabling her to champion the integration of AI and digital innovation into regulatory and quality practices. She is recognized for driving transformative approaches that enhance compliance efficiency, accelerate market access, and position the MedTech industry to meet the challenges of a rapidly evolving digital landscape.