5^th Annual European Medical Device Human Factors and Usability Engineering Conference

We Interact Together Innovate Together Inspire Together.

Advancing Human Factors: Driving User-First Solutions, Regulatory Compliance, and Strategic Innovation

Key Topics for 2025

Global perspective on HF regulation: A review of emerging standards and compliance strategies
Through a Notified Body’s Lens: Usability Engineering Documentation Key Expectations, Common Issues, and Practical Tips for Success
Reducing inefficiencies in the design and user testing cycle through better integration
Critical HF considerations and compliance strategies for navigating MDR approval including post-market updates of software-based & AI-based medical devices
Defining "Good Enough" testing: Establishing practical thresholds for testing while meeting regulatory requirements
Bridging disciplines for enhanced HF processes: Why integration with clinical, medical affairs, risk management, and regulatory teams matters
Adaptive simulation environments: Accounting environmental factors and customizing testing conditions to reflect diverse clinical scenarios
Exploring the complexity in multi-user scenarios in human factors testing: Strategies for process improvement
Scaling Use-Related Risk Analysis in HFE: Practical challenges and best practices
Identifying and preventing typical usability engineering non-conformities: A guide for manufacturers
Leveraging Real-World Evidence in Human Factors: Utilizing Post-Market Data to Improve Device Usability

Why Attend a TT Conference

Maximum Engagement

Meet our 2025 Conference Speakers

Maurizio Sacchero

Medical Device Lead Auditor - Technical Developer

SGS ITALIA

Alexandra Zahn

Director Humanizing Healthcare Design, Senior Key Expert Patient & Staff Experience

SIEMENS HEALTHINEERS

Fie Falck Larsen

Senior Usability Engineering Lead

NOVO NORDISK A/S

Shaloo Sood

Team Leader RDI Academy

INSTITUT STRAUMANN AG, BASEL

Linda de Valk

Senior Usability Engineer

Philips

Targeted Content

With our targeted attendee and speaker line-up, you can have meaningful conversations with industry-specific experts who have faced the same situations and challenges. Spark new ideas by brainstorming during our breakout sessions, informal post-session Q&As, panel debates, case studies, and workshops.

Meet Industry Leaders

Our robust screening process ensures an exclusive environment where you can focus on connecting and fostering stronger working relationships with those in the medical device field. Collaborate to find the necessary solutions to your current problems.

Customize Your Content

Get the most out of this event experience by choosing what content is most relevant for you and your company and tailoring your event experience around this decision. Learn and connect with whomever you want, whenever you want, and however you want.

If you are a part of the Medical Device Human Factors and Usability Engineering community, TT Human Factors guarantees a valuable return on time invested.

The TT Sales & Clinical Training Conferences provide a unique opportunity for Medical Device industry professionals to collaborate and gain practical insights into overcoming challenges related to ensuring patient safety and meeting regulatory requirements. With expert speakers from leading regulatory bodies, manufacturers, and technology innovators, attendees will benefit from actionable takeaways, real-life business examples, and opportunities to network and stay abreast of emerging trends and evolving requirements.