Upcoming & past events
Webinar | Off-label? Don't panic: A strategic approach to real-world data
When approached strategically, RWD can help confirm long-term safety and performance, strengthen your clinical evidence base, support label expansions, and identify unmet clinical needs. The challenge lies in building a framework that is both methodologically robust and proportionate to your device and regulatory context..
Webcast | Cracking complex MedTech decisions: How SIMALTO reveals what truly drives stakeholder choice
SIMALTO (Simultaneous Multi-Attribute Level Trade-Off) can be used to transform MedTech market research by tackling one of the industry's biggest challenges: understanding complex, multi-factor decision making among healthcare stakeholders.
Webcast | The Global Shift in Real-World Evidence: Insights from MedTech Industry Leaders
Real-World Evidence (RWE) is playing an increasingly important role in global MedTech regulatory decision-making, supporting evidence generation across the product lifecycle, from pre-market submissions to post-market surveillance. Watch this webcast which features industry experts to understand how MedTech manufacturers can build effective, compliant RWE strategies.
Webcast | Medical devices in the wild: Tracking real world data for lasting impact
Join expert presenters; Breda Kearny - Clinical Regulatory Lead, BSI, Diane M. Legere - Senior Clinical Auditor, DNV, Marcus Torr - Head of Post Market Surveys, Purdie Pascoe and Efsthathios Vassiliadis - CEO, Evnia for this insightful live event on Wednesday 10 September, 2025.