RAPS EU Convergence 2026
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Event details
QbD Group, your life sciences partner across the entire product lifecycle
At MEDICA 2026, our experts will share practical insights on navigating evolving global regulatory frameworks and clinical trial requirements. From international collaboration pathways to upcoming UK regulatory changes, we help you align strategy, compliance and execution across markets:
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International Regulatory Collaboration & Project Orbis – Leverage regulatory reliance and work-sharing pathways through real-world experience with FDA Project Orbis and emerging global collaboration models such as the UK–Singapore corridor.
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Navigating Global CTR–IVDR Trials – Align drug–diagnostic development across Europe, the UK and the US by addressing IVDR clinical obligations and operational challenges in combined trials.
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New UK Clinical Trial Regulations – Prepare for the April 2026 UK CTR update with clarity on authorisation changes, approval timelines and strategic implications for sponsors.
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Additional Session – A fourth expert session is currently being finalised.
Connect with our team of experts
Stop by and connect with our experts! Whether it’s regulatory guidance, market access strategies, or quality systems, we’re here to help you navigate the fast-changing healthcare landscape. Visit us at the exhibition or reach out today to see how we can accelerate your success in medical innovation.
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Get in touch
Have a question or need more information? We’re here to help! Fill out the form and our team will get back to you as soon as possible.
Let’s start the conversation!
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