7^th Annual European Medical Devices
Post-Market Surveillance & Vigilance Conference

We Interact Together. Innovate Together. Inspire Together.

Ensuring Safety: Proactive Approaches to Post-Market Surveillance and Vigilance Across the Product Lifecycle

Conference Highlights

Pre-Workshops & Roundtable Sessions

Engage in interactive discussions on:

Post-Market Clinical Follow-Up (PMCF) in the EU & GB: Navigating Compliance and Effective Strategies
MDSAP Vigilance Requirements in Field Safety Corrective Actions (FSCA): Best Practices
Harmonizing IMDRF Codes Across Global Regulations: Challenges Effective Approaches
PMS Reports vs. PSUR: Drawing parallel and what’s Next?
From Detection to Action: Streamlining response protocols in vigilance
Lessons learned from real-world recalls and adverse event handling
Global Perspectives: Aligning Complaint Management and PMCF Across Markets

Conference Sessions

Attend insightful presentations covering:

Practical PMS for best PSUR compliance
Managing Compliance with PMS Requirements for Great Britain and the EU
Integration of AI in Post-Market Surveillance (PMS): Benefits & Challenges
Trend Reporting According to Article 88 Of EU MDR
Global Perspectives: Aligning Complaint Management and PMCF Across Markets
Clinical Evaluation Strategies of High-Risk Implantable Devices: Current State of Play
The Feedback Loop: How PMS Feeds Risk Management

Why Attend a TT Conference

Maximum Engagement

Notified Body Speakers

Carolina Peetz

Clinical Reviewer - Internal Clinician

TÜV SÜD

Dr Gavin Quigley

Senior Internal Clinician

BSI

Jenifer Hannon

Post Market Surveillance Regulatory Lead

BSI

Omar Abou Ezzeddine

Technical Team Manager

BSI

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.