DIAmond Sessions

Environmental Sustainability

Explore the adaptation of R&D, CMC, quality control, and clinical research towards environmental sustainability. Discover new sustainable opportunities across the healthcare product development continuum.

EU Regulatory Townhall

Join a conversation with EMA and European Commission representatives on the promises and challenges of the new EU Pharma Legislation. Discuss the progress since the EU elections and the steps towards adopting the new legislation.




Patient Engagement

Learn about the current consensus on the inclusion of patient experience data at different stages of healthcare product development. Review recent successes in patient engagement and identify meaningful future opportunities.




Europe: Pioneering a Global Digitalization Strategy for Medicine Regulation

Join us as we examine Europe’s pivotal role in leading the global digitalization of medicine regulation. We’ll explore Europe’s unique position in the global healthcare landscape, the transformative benefits of digitalization, and the challenges we face in implementing it. We’ll discuss strategic approaches to overcome these hurdles, including the EMA/HMA vision of a regulatory system that harnesses AI for efficiency and improved decision-making. Finally, we’ll highlight the power of collaboration and harmonization in creating digital regulation solutions. This session offers a blueprint for global adoption, paving the way for a more efficient, transparent, and patient-centric regulatory ecosystem.




The Future of Innovation: Europe of Possibilities

Discover what fuels Europe’s innovation engine. This session discusses the diverse stakeholders that make up the European innovation ecosystem, including R&D, manufacturers, regulators, payers, and patient representatives. We’ll discuss how efficient R&D and robust supply chains contribute to Europe’s global leadership in technological platforms and innovation. We’ll also navigate the complex landscape of Europe’s policy pillars and the reforms proposed by the European Commission. Join us as we examine opportunities to strengthen European innovation and address key concerns such as access, affordability, and availability of medicines.




Regulatory Agility, Convergence and Harmonization

Join a dynamic discussion on the harmonization of global standards and the convergence of regulatory processes. Understand how these elements support international collaboration, enabling quicker access to medicines for patients worldwide. With the rapid pace of technological innovation and increasing regulatory workload, discover how regulators are implementing reliance models for various activities. Join WHO, global regulators, and industry stakeholders as we explore the practical aspects of collaboration and discuss strategies to drive broader implementation of collaborative pathways for sustainable healthcare systems.