
US Edition Medical Device & Diagnostic Supplier Quality Management Conference
Collobration, Innovation, Excellence: Shaping the Future of Supplier Quality
- 18th - 20th November
- US
We Interact Together. Innovate Together. Inspire Together.
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
- 20+ Expert Speakers Sharing Cutting-Edge Insights
- 07 Hours of Networking
- 3 Days of Engaging Content
- Networking Opportunities
- Practical & Theoretical Case Studies
Maximum Engagement
- Pre-Workshops
- Roundtable Discussions
- Panel Discussion
- Speed Networking Sessions
- Presentations
Our Industry Specialists

Neela Bhargavi Ganduri
Director, Supplier Quality and Development
GE Healthcare

Sarah Coviaux
Global Services Department Manager and Lead Auditor
GMED North America

Tony Kimble
Regulatory Lead Auditor
(MDSAP, ISO 13485, MDR)
Dekra

Jetzabeth Deliz
Former QA Director
BD

Kathy Lyall
Director, SQ Processes & Systems
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.