European Medical Device Summit 2025

Start:

Tue, 3 Jun 2025, 09:00

End:

Wed, 4 Jun 2025, 18:00

Website:

https://iii.hm/emds2025

Venue:

Exhibit

Symposia

Workshops

Organiser

Sponsor

The European Medical Device Summit is a leading medtech event in Düsseldorf, offering actionable strategies to advance medical device development, design, product development technologies, and regulatory affairs.

Join over 120 fellow medical device leaders to explore advanced medical device technologies such as eQMS, continued process verification (CPV), and regulatory reporting. Hear from some of the largest medical technology companies on QMS management, ISO standards for medical devices, and change management in digital transformation.

Gain insights to streamline medtech design and sustainability, mitigate risks, reduce costs, accelerate time-to-market, and ensure compliance with European medical device regulations, such as EU MDR. Discover advancements in AI in medical devices, IoMT, product development, and medical technologies while tackling challenges in manufacturing medical devices, digital transformation, and managing clinical trials.

Key Themes

Minimizing initial investments and mitigating risks by incorporating frequent medical device prototyping during the early phases of medical device product development ensures a more efficient and reliable pathway to innovation.
Driving medical device innovation and optimizing the design and development of medical devices enables a smoother transition into production, ensuring efficiency and faster time-to-market.
Integrating performance, safety, and business economics as foundational pillars in medical device research and development ensures a streamlined and efficient approach to medical device manufacturing, driving innovation while meeting industry standards and market demands.
Leveraging SaMD (Software as a Medical Device) to drive medical device innovation, improve QMS, drive patient outcomes, and meet evolving regulatory requirements.

Quality & Regulatory

Recognizing hurdles and opportunities across regulatory markets, addressing EU MDR deadlines, and aligning with Europe’s medtech standards.
Ensuring compliance with QMS quality management frameworks and continuous process verification (CVP) for seamless operations.
Utilizing digital transformation in healthcare to revolutionize medical device design, streamline manufacturing processes, and enable data-driven decision-making throughout the product lifecycle.