7th Annual European Medical Device & Diagnostic Quality Assurance and Regulatory Affairs Conference
- 26th & 27th November 2024
- Sheraton Airport Hotel | Brussels, Belgium
We Interact Together. Innovate Together. Inspire Together.
Unlock tomorrow's standards today: Innovate, collaborate, and lead at the Quality Assurance and Regulatory Affairs Conference!
Key Topics for 2024
- Effective strategies to overcome QMS integration challenges in accordance with the MDR
- ISO 13485:2016 – quality management system requirements for regulatory purposes in the EU and US
- How to make inspections effective for continuous quality improvement
- Leveraging artificial intelligence for regulatory submissions
- How does quality culture contribute to compliance?
- Notified body perspective: addressing IVDR certification challenges
- How to manage the quality of software as a medical device
- Managing your importers and distributors in line with the MDR expectations
Why Attend a TT Conference
- 60+ Professionals from the Medical Device QA & RA Department only!
- 15+ Solution-Focused Sessions
- 07 Hours of Networking
- A Limited Number of Attendees
Maximum Engagement
- 04 Roundtable Discussion
- 02 Interactive Workshops
- 02 Days of Knowledge Sharing
- 01 Speed Networking Session
- 01 Panel Discussion
- 01 Fireside Chat
Our Industry Specialists
Marta Carnielli
Head Of Certification IVD
TÜV SÜD PRODUCT SERVICE GmbH
Martin Geertsema
Sr Director QA & RA International
CONMED
Dr Zulfiyya Hasanov
Commercial Quality EMEA
ABBOTT
Massimo Terrin
QARA Manager
AGFA HEALTHCARE NV
Dr Stefanie Meyer
Quality Manager
ESSITY
Ella Helgeman
Regulatory and Quality Director
REHALER A/S
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 and Diagnostic Quality Assurance & Regulatory Affairs community, TT QARA guarantees a valuable return on time invested.
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