6th Qserve MedTech Conference - General and Startups
Taking place from 10 to 12 November 2026 in Amsterdam, the 6th Qserve MedTech Conference brings together the brightest minds 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 General and Startups: A two-day conference on ππβππ ππ¨π―ππ¦πππ«, ππππ, featuring plenary sessions, expert panels, and 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 General and Startups Track consists of 5 sessions divided over two days. On day 1 there will be two sessions covering topics like QMS and Engaging with Regulators On day 2 there will be three different sessions, including themes like Startup survival guide, clinical challenges for startups and real cases about submission success.
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 General and Startups Track consists of 5 sessions divided over two days. On day 1 there will be two sessions covering topics like QMS and Engaging with Regulators On day 2 there will be three different sessions, including themes like Startup survival guide, clinical challenges for startups and real cases about submission success.
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 - QMS That Works: Building Systems That Truly Add Value
A Quality Management System should enable, not hinder, your organization. This session focuses on building and maintaining a QMS that drives efficiency, compliance, and continuous improvement.
You will learn how to move beyond βcheck-the-boxβ compliance and create a system that supports your teams and business goals.
Session 2 - Engaging with Regulators: How to Maximize Value from Interactions
Effective communication with regulatory authorities can significantly impact your success. This session provides practical guidance on how to prepare for and manage interactions with regulators and notified bodies.
You will learn how to ask the right questions, present your case clearly, and build constructive relationships.
Session 3 - Start-Up Survival Guide: Overcoming Regulatory Challenges
Start-ups face unique regulatory hurdles. This session focuses on the most common challenges and practical solutions to overcome them efficiently.
You will learn how to prioritize resources, build a scalable regulatory strategy, and avoid costly mistakes.
Session 4 - Clinical Challenges for Start-Ups: From Evidence to Approval
Generating clinical evidence is one of the biggest hurdles for start-ups. This session explores practical strategies to design and execute clinical activities efficiently.
You will learn how to align clinical strategy with regulatory requirements while managing limited resources.
Session 5 - Submission Success: Lessons Learned from Real Cases
What makes a submission successful? This session shares real-world lessons learned from regulatory submissions, highlighting common mistakes and best practices.
You will gain practical insights into how to build a compliant and effective submission file.
General and Startups
Across 5 sessions, explore how evolving regulations, AI, and software-driven innovation are reshaping compliance and market access for digital health technologies.
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.
Clinical
In 5 sessions, discover best practices for clinical strategy, PMCF data collection, PMCF surveys with real-world data and more.
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.