Join Qualtech's Webinar on 2025 Regulatory Updates & Forecast for Chinese Medical Device Regulations

Join us on May 27th for an exclusive webinar hosted by Qualtech China team. We’ll provide authoritative insights into China’s evolving medical device regulatory framework. As China implements the “Healthy China 2030” initiative, the medical device market is entering a golden era of growth.

But the implementation of the revised Medical Device Supervision Regulation, expansion of Marketing Authorization Holder (MAH) trials, and evolving compliance requirements for digital health products are reshaping market access – presenting new challenges for both domestic innovators and multinational corporations.

 

You'll gain crucial insights on:

• Get Ready for NMPA Registration: Prepare Your Dossier for Success
• Decoding Technical Review: Navigating the Evaluation Process
• Post-Market Surveillance Rules: In-depth Expert Explanation
• China Regulatory Insights: Practical Tips from Our Experts

 

Webinar details:

• Date: Tuesday, May 27, 2025
• Time: 4 PM (GMT+8) / 10 AM (CET)
• Language: English
• Register here: https://forms.gle/RzzCcArbKnYSboBM7

 

Secure your spot for our webinar and interact with our exclusive professional speaker.

 

We look forward to seeing you there!

 

If you have any questions, feel free to contact us at globalra@qualtechs.com