Deep Dive into China's Medical Device Regulatory Market: A Comprehensive Guide

July 3, 2024

50 Minutes

Join the Webinar as per Your Time Zone

For AMR & EU

10:00 AM EST | 04:00 PM CET

For RoW

11:00 AM IST

What is it all about?

China’s medical device market is rapidly evolving with significant Regulatory reforms aimed at improving the medical devices safety and quality standards. Compliance with China's evolving Regulatory landscape is paramount for medical device manufacturers to sidestep potential penalties for non-compliance. Do you comprehend Chinese Medical Device Regulatory dynamics, relevant regulations, and various device registration procedures as a device manufacturer? Why is it important for medical device manufacturers to develop a robust strategy for navigating the Chinese Regulatory framework?

To assist you in better understanding the wide Regulatory landscape of the Chinese Medical Device industry and guide you through the intricacies of China's medical device regulations, we are presenting you with an exclusive webinar on "Deep Dive into China's Medical Device Regulatory Market: A Comprehensive Guide."

The webinar will be hosted by Sushil Bhatt, and our in-house Regulatory expert - Summer Xia will elaborate on:

  • China Medical Device Industry - Background.
  • The Chinese Medical Device Regulatory Landscape.
  • The Factors Affecting Medical Device Registration in China.
  • Detailed Registration Process for Medical Devices in China.
  • Freyr Success Story.
  • FAQs.

Given the keynotes and with due consideration for your hectic schedule, we anticipate seeing you in the webinar. Register now! Stay informed. Stay compliant.


Sushil is a seasoned strategist with five (05+) years of experience in Medical Device, Healthcare, and FMCG sectors. He holds a BE and MBA from BITSoM and is certified in ISO 13485 audit and Lean Six Sigma Green Belt from TUM Munich. He is proficient in Go-to-Market strategies, key account management, and team building. He excels in assisting clients to enter new markets and offers comprehensive Regulatory solutions, developing customized strategies that enhance organizational value.


With over twenty (20) years of experience, including fifteen (15) years in medical device Regulatory affairs, Summer has excelled in navigating both pre-market and post-market requirements. Her expertise has been instrumental in guiding numerous foreign and local manufacturing companies entering the Chinese market. Summer’s leadership has been demonstrated through her roles heading multinational quality assurance and Regulatory affairs teams. She holds an MBA and is a certified Lead Auditor by BSI, enabling her to proficiently manage complex compliance landscapes.


Sushil Bhatt

Deputy Manager- Europe & Africa, Freyr Solutions


Summer Xia

Associate Director- Medical Devices, Freyr Solutions (China)