6th Qserve MedTech Conference - Clinical
Taking place from 10 to 12 November 2026 in Amsterdam, the 6th Qserve MedTech Conference brings together the brightest minds in Clinical to help you stay ahead in an ever-evolving landscape.
Weβre pleased to announce the return of the Qserve MedTech Conference, a must-attend event for MedTech professionals navigating an evolving global regulatory landscape.
π Amsterdam, The Netherlands
π 10-12 November, 2026
ππ‘ππ ππ¨ ππ±π©πππ of Clinical: A two-day conference on ππβππ ππ¨π―ππ¦πππ«, ππππ, featuring plenary sessions, expert panels, and multiple parallel tracks with in-depth discussions on key regulatory and industry topics.
By combining regulatory insight, hands-on experience, and real-world industry challenges, the Qserve MedTech Conference offers valuable opportunities to deepen your expertise and connect with others. Further details on the program, speakers, and key topics will be shared in the coming months.
We look forward to welcoming you to Amsterdam for the #QserveMedTechConference. Sign up now and check the schedule!
The Clinical Track consists of 5 sessions divided over two days. On day 1 there will be two sessions covering topics like High-Risk Clinical Investigations and Clinical Evaluations. On day 2 there will be three different sessions about Data-management, PMCF Surveys and alignment of multiple clinical processes.
Not only will our own Qserve experts take the stage to tell you about these topics in-depth, Notified Bodies and relevant Industry Speakers will join these sessions. Stay tuned for more information on the external speakers.
Each session lasts 1,5 hour. Please make sure to be at the location before the session starts.
The Clinical Track consists of 5 sessions divided over two days. On day 1 there will be two sessions covering topics like High-Risk Clinical Investigations and Clinical Evaluations. On day 2 there will be three different sessions about Data-management, PMCF Surveys and alignment of multiple clinical processes.
Not only will our own Qserve experts take the stage to tell you about these topics in-depth, Notified Bodies and relevant Industry Speakers will join these sessions. Stay tuned for more information on the external speakers.
Each session lasts 1,5 hour. Please make sure to be at the location before the session starts.
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Read more about our sessions
Session 1 - High-Risk Clinical Investigations: Lessons from a Novel Heart Valve Case
High-risk clinical investigations require careful planning and execution. This session shares real-world experience from a novel heart valve case.
Session 2 - Clinical Evaluation for Software & AI Devices
Clinical evaluation for software and AI devices requires a tailored approach. This session provides practical guidance on demonstrating clinical performance and safety.
Session 3 - Software, AI & Risk Management
Collecting PMCF data is often seen as resource-intensive and complex, yet much of the required data already exists within your organization or can be captured with minimal additional effort.
This session focuses on how to design efficient, low-burden PMCF strategies that deliver meaningful clinical evidence while staying compliant with MDR and IVDR requirements. You will learn how to leverage existing data sources such as PMS data, complaints, literature, and registries, and how to integrate PMCF activities into routine processes.
Through practical examples, we will show how to reduce effort, avoid over-engineered studies, and still meet regulatory expectations for clinical evidence and CER updates.
Session 4 - PMCF Surveysβ Minimum effort, Maximum output!
PMCF surveys are a key tool for real-world data collection. This session focuses on designing and implementing effective surveys.
Session 5 - Closing the Loop: PMS, PMCF, Risk Management & Clinical Evaluation
Post-market surveillance, PMCF, risk management, and clinical evaluation are deeply interconnected. This session explains how to align these processes effectively.
General and Startups
Through 5 sessions, gain practical insights into regulatory strategy, funding and scaling challenges tailored to emerging MedTech companies and innovators.
In-Vitro-Diagnostics
In two focused sessions, understand the latest developments in IVDR compliance, from performance evaluation to lessons learned from CDx submissions.
Global Registrations
Over 3 sessions, learn how to efficiently navigate international regulatory pathways and accelerate market access across key global regions.
Digital Health
Across 5 sessions, explore how evolving regulations, AI, and software-driven innovation are reshaping compliance and market access for digital health technologies.
Demonstrations
Across 3 live demonstrations, experience Qserve Learn, Qserve InSight and AI Clinical in action, showcasing solutions to streamline training, regulatory intelligence, and clinical processes.
Choose Your Conference Experience
Pre-Conference Workshop Ticket
Join our hands-on pre-conference workshops on 10 November 2026 and gain practical insights through focused sessions designed to prepare you for the latest MedTech regulatory challenges.
Conference Ticket
Attend the two-day conference on 11 and 12 November 2026 to access expert-led sessions, industry insights, and valuable networking with MedTech professionals.
Full Conference Ticket
Get the complete experience with access to both the pre-conference workshops on 10 November and the full two-day conference on 11 and 12 November 2026.
We offer group tickets and special offers, contact training@qservegroup.com for more information.
We offer group tickets and special offers, contact training@qservegroup.com for more information.