search
Englishexpand_more
No other languages available
Contact us
search
ENG
No other languages available for now
Contact us
Blog Hero
Blog

Meet and Greet Qserve Experts at the European Medical Device Summit 2026

Qserve is proud to be a Gold Partner at this year’s European Medical Device Summit, Europe’s premier event for medtech professionals. Join us as we connect with over 200 industry leaders to explore the latest in medical device innovation, regulatory strategies, and product development technologies. 

Date: 9-10 June 2026

Location: Maritim Düsseldorf, Germany

Introduction

Qserve is proud to be a Gold Partner at this year’s European Medical Device Summit, Europe’s premier event for medtech professionals. Join us as we connect with over 200 industry leaders to explore the latest in medical device innovation, regulatory strategies, and product development technologies.

Meet our experts at our booth: Jan van Lochem, Iris Verboven, and Celien van Lochem will be on-site to discuss your challenges and share insights on:

  1. Strategic regulatory and compliance support – expert guidance on regulatory affairs, market access planning, CE marking, and submission support that aligns with evolving EU MDR/IVDR and global regulatory frameworks, enhanced by Qserve InSight for up‑to‑date regulatory intelligence.
  2. Quality management and assurance services – practical QA support, QMS gap assessments, audits, and interim quality resource solutions to strengthen QMS performance and support design, development, and compliance objectives.
  3. Clinical research and data strategy – design and execution of clinical investigations, PMCF services, surveys, and performance evaluation activities to generate robust clinical evidence and meet regulatory requirements.
  4. Targeted training and capability building – tailored courses and professional development through Qserve Learn, covering regulatory, quality, and clinical topics to empower teams with actionable expertise.
  5. Interim and flexible resourcing solutions – support your internal teams with interim experts or project‑based resources across regulatory, quality, and clinical functions to keep momentum in fast‑moving development programs.

Hear from leading medtech companies on QMS management, ISO standards, continued process verification (CPV), and regulatory reporting. Gain actionable insights to tackle challenges in manufacturing, clinical trials, and sustainable medical device design.

We look forward to seeing you there. More information about the event can be found on the European Medical Device Summit website.