MedDev Day

MedDev Day 2026 - Building Opportunities in the EU Single Market

Clearer rules. Smarter pathways. Stronger innovation.

MedDev Day 2026 takes place at a decisive moment for professionals working with medical device regulation in Europe.

As the EU advances major initiatives to strengthen the Single Market, simplify MDR/IVDR implementation, and improve regulatory efficiency, medical device professionals are facing significant change - and equally significant opportunity. MedDev Day 2026 is designed to help you understand what is changing, why it matters, and how to respond with confidence.

In 2026, the European regulatory landscape will evolve through concrete, practice-shaping developments:

• New secondary legislation for well-established technologies and notified body requirements
• Publication of Commission Implementing Regulation (EU) 2026/977, improving procedures for conformity assessment under the EU MDR and IVDR
• Implementation of coordinated clinical investigation assessments
• Mandatory rollout of key EUDAMED modules
• Targeted MDR/IVDR amendments and governance reforms
• EU's broader better-regulation and competitiveness agenda reshaping medical technology development

Key Conference Topics

MedDev Day 2026 brings together regulatory leaders, industry experts, notified bodies, and policymakers to translate these regulatory changes into practical insight.
The programme focuses on what these reforms mean for regulatory strategy, compliance planning, clinical evidence generation, and lifecycle management — with a clear emphasis on reducing unnecessary administrative burden, improving predictability, and supporting high-quality innovation.

More than a policy discussion, MedDev Day 2026 is a learning and exchange platform for professionals who need clarity, foresight, and actionable guidance.

Join us to explore how Europe can remain the most attractive environment to develop, assess, and bring medical technologies to patients — and how you, as a regulatory or quality professional, can navigate the next phase of the EU framework effectively.

Scientific Board

Bassil Akra, Chief Executive Officer at AKRA TEAM
Arkan Zwick, Director Regulatory Affairs

Who should attend MedDev Day 2026?

MedDev Day is designed to give medical device professionals the clarity, confidence and practical understanding needed to navigate the next phase of EU regulation.
The event is particularly relevant for professionals in:

• Regulatory Affairs
• Quality Management
• Clinical Operations and Clinical Affairs
• Medical Affairs
• Post-Market Surveillance and Vigilance

working across medical device and IVD manufacturers, pharmaceutical and biotechnology companies, Contract Research Organisations (CROs), notified Bodies, universities, hospitals, and academic research organisations, patient associations and healthcare organisations, competent authorities and EU institutions.

Whether you're managing regulatory submissions, coordinating clinical trials, or ensuring post-market compliance, MedDev Day 2026 provides the strategic insights you need.

MedDev Day - Building Opportunities

MedDev Day 2026 is the European reference conference for professionals working with medical device regulation. The event delivers practical updates on MDR, IVDR, EUDAMED, and EU Single Market reforms planned for 2026, with an operational focus for Regulatory Affairs, Quality Management, and Clinical Operations teams.

Organized by LS Academy, a leading provider of pharmaceutical and medical device training and conferences since 2010, MedDev Day 2026 brings together regulatory leaders, notified bodies, and industry experts to translate complex regulatory changes into actionable strategies.