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MedTech Summit
15 - 18 June 2026
JW Marriott Hotel Berlin, Berlin, GermanyAttend In-Person or 100% Digitally

Find Your Path

Clinical & PMS Professionals

Gain actionable insights into clinical evaluations and PMS guidance updates. Learn from case studies, join stakeholder conversations, and connect with regulatory authorities to streamline your approach.

Expert Insights, Tailored Networking, and Cutting-Edge Solutions Designed for Professionals Like You

MedTech Summit 2026 is the go-to event for Clinical & PMS Professionals seeking to navigate the complexities of clinical evaluations and post-market surveillance. Hear from industry leaders and peers about their approaches to guidance updates, cross-legislation impacts, and global reliance strategies.

Participate in practical case study sessions, stakeholder conversations, and roundtable discussions to gain actionable insights and streamline your approach. Connect with notified bodies and regulatory authorities to stay ahead of the curve and network with the wider MedTech regulatory community.

Customised Programmes to Drive Innovation and Success

Clinical Evaluations & PMS

Dive deep into the latest guidance updates, cross-legislation impacts, and global reliance strategies. Learn how to optimize clinical evaluation and PMS processes to enhance patient safety and regulatory compliance.

European Regulatory Affairs

Gain clarity on the EU Medical Device Regulation and its implications for clinical evaluations and PMS. Understand how MDR requirements shape your responsibilities and strategies.

Patient Access & Reimbursement Workshop

Explore the intersection of clinical data and market access. Learn how robust clinical evaluations and PMS can support reimbursement strategies and improve patient access.

Future Regulatory Leaders Linkup

Connect with emerging leaders in the regulatory space. Share insights and build relationships that can drive innovation and collaboration in clinical and PMS practices.

Clinical Evaluations & PMS Roundtable

Engage in focused discussions with peers, notified bodies, and regulatory authorities. Share experiences, challenges, and solutions to refine your approach to clinical evaluations and post-market surveillance.