Date: 1-3 September, 2026
Location: Shanghai New International Expo Center, China
Introduction:
Currently, the global medical device regulatory landscape is becoming increasingly stringent, with the FDA’s rigorous oversight becoming the norm and domestic regulations continuously evolving. Whether it involves product registration, quality control, testing and certification, or system development, companies are confronted with heightened compliance demands. The cost of non-compliance has risen significantly, and cases of severe market setbacks due to compliance failures serve as a stark warning to the industry.
The MedTec Quality and Regulatory Conference helps medical device companies in addressing compliance challenges, accelerating time-to-market, and surmounting obstacles throughout the entire compliance and commercialization process. Focusing on core compliance needs, the conference brings together top-tier industry service providers to establish a targeted matchmaking platform, empowering companies to achieve efficient product compliance and market entry.
Session Details | The 7th Regulatory Lecture: Solutions to Acelerate the Compliance and Market Launch of Medical Device Products
- Topic: Latest Updates to the 2026 EU MDR Regulation
- Location: Meeting Room E, Hall N4, Shanghai New International Expo Centre
- Date: September 2, 2026 | 10:30 - 11:00
For more details, and the full agenda, visit the event website.
Shanghai New International Expo Center
01 September 2026
02 September 2026
03 September 2026

