Meet DNV in April 2026: CMEF & Customer Seminar

April will be an exciting and engaging month for DNV, with both our participation in a major industry exhibition and a dedicated customer seminar in Shanghai. We look forward to connecting with medical device professionals, sharing regulatory insights, and discussing how we can support your compliance journey.

DNV at CMEF 2026

DNV will participate in the China International Medical Equipment Fair (CMEF) 2026, one of the world’s leading platforms for the medical device industry.

The exhibition brings together manufacturers, regulators, healthcare providers, and industry experts to showcase innovations and exchange perspectives on regulatory developments and market trends.

During CMEF, DNV experts will be available to discuss:

  • EU MDR certification and regulatory updates 
  • Post-market surveillance and technical documentation expectations 
  • Strategies for entering and sustaining access to the European market 
  • Compliance challenges and practical solutions for medical device manufacturers 

We invite you to visit our booth to meet our team and explore how DNV can support your regulatory and certification needs.

Event details

  • Dates: 9 – 12 April 2026
  • Venue: CMEF 2026
  • DNV Booth: H7.1 – T18, U17, U18

DNV Customer Seminar: Medical Device Compliance in Practice

In addition to CMEF, DNV will host a dedicated customer seminar in collaboration with CMD (Beijing Hua Guang Certification of Medical Devices) and Blue Balloon (Beijing) Medical Research.

With increasing regulatory scrutiny and evolving international requirements, this seminar is designed to help companies strengthen their understanding of key compliance topics and enhance their practical capabilities in regulatory implementation.

The session combines regulatory interpretation with real-world application, providing actionable insights across the lifecycle of medical devices. (detailed program below)

Event details

  • Date: 7 April 2026
  • Time: 13:30 – 17:00
  • Location: DNV Shanghai Office

Join us

Whether you are attending CMEF or joining our seminar in Shanghai, we welcome the opportunity to connect with you.

Meet our experts, discuss your regulatory challenges, and learn how DNV can support your journey towards compliance and market access in Europe.

We look forward to seeing you in April!

Agenda

DNV Customer Seminar: Medical Device Compliance in Practice

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Module 1: EU Medical Device Post-Market Surveillance

 

  • Overview of the EU medical device post-market surveillance system
  • Core regulatory requirements for PMS / PMCF / PSUR
  • Compliance requirements for the Eudamed database
  • Enhanced EU post-market surveillance requirements for 2026
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Module 2: Integrating Regulations and Risk Management into Design & Development

 

This session focuses on aligning product development with regulatory and risk management requirements.

  • Design and development process for active medical devices
  • Verification and validation in design and development
  • Design, development, and risk control
  • Regulatory requirements for active medical device design and development under the 2025 GMP
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Module 3: ISO 18969 Clinical Evaluation Methodology

 

Focusing on the international standard ISO 18969:2025 for clinical evaluation of medical devices, this session clarifies its role as a methodological tool supporting MDR and MDCG, breaks down execution processes across the full lifecycle of clinical evaluation, and outlines key requirements such as evidence quantification, reference framework construction, and bias control. It also provides practical recommendations for companies to prepare in advance for EU regulatory compliance and optimize clinical strategies.