New update on China NMPA Regulation and Registration for Medical Devices with Case Studies

You will get a deep understanding of the up-to-date China NMPA regulatory policies.

Course objective and outcome

Chinese market becomes more and more important for medical device manufacturers due to its large volume. The NMPA registration process is very time and cost consuming. Also, China NMPA is updating the regulations very rapidly recently.

This course aims to provide the participants a deep understanding of the up-to-date NMPA regulatory policies and practical solutions to the problems of frequent occurrence during Chinese market entry.

Content

  • NMPA organization reform and regulation system
  • Important concepts for NMPA registration
  • Product registration III
  • “Made in China” Strategy: Registering a domestic device
  • Vigilance and inspection
  • Registration renewal and change
  • Green channel for innovative device and prioritized device

Who should attend

This course is suitable for not only RA and clinical professionals who manage the product approval work, but also international marketing and C-level directors who are interested in Chinese marketing strategy.

Trainer

Dr. Chao Xu, Director of International Business, Keuro Solutions

What previous participants said

“Chao was great at presenting the updates to the chinese, as well as mentioning the nuances of the requirements and how these are interpreted”

“I liked the capability of the course leader and the content of the course”

“The Instructor was quite experienced and could bring theory and practice together”

“Great speaker with deep knowledge in the subject”

Contact

Morten Petersen

Morten Petersen

Uddannelseskonsulent

49 18 47 03
mp@medicoindustrien.dk

Select date

1-2.10.2026

1-2 October 2026 - at 09:00 - 16:00

Price ex. VAT
Member price: 12.900 DKK
Other: 19.840 DKK

Latest Registration
28.09.2026
Latest Cancellation
01.09.2026

Address
Medicoindustrien
Bøge Allé 5, 2. th
2970 Hørsholm

Register

View Program
Terms

In-house Courses

MedTech Academy offers in-house training courses tailored to your specific needs. Courses can be based on our open programme or developed specifically for your organisation. You choose the focus, format and timing – and work with your own cases in a confidential setting. Contact us to discuss the possibilities.

In-house courses for medical device companies

Do You Have a Specific Competency Need?

We continuously develop and update MedTech Academy’s course portfolio to match the current needs of medical device companies. If you are looking for a specific course, or if you are unsure which course is the right fit for you and your organisation, you are always welcome to contact us.

Berit Munkebo
Head of Development
bm@medicoindustrien.dk

Academy News

Academy News is Medicoindustrien’s weekly newsletter with a complete overview of upcoming and newly developed courses from MedTech Academy. The newsletter provides a quick overview of new dates, upcoming sessions and current course topics for professionals working with medical devices.

Sign up for our Academy News newsletter

Nyhedsbrev formular