##  [Decoding China's Marketing Authorization Holder (MAH) System](/index%2ephp/webinars/decoding-chinas-marketing-authorization-holder-mah-system) 

![Decoding China's Marketing Authorization Holder (MAH) System]()

<a>Pharmaceuticals</a>



<a>Past Webinar</a>



## **Decoding China's Marketing Authorization Holder (MAH) System**

**The webinar was successfully concluded on**

  **March 06, 2024**

[Download Webinar](javascript:void(0))







#### **Topics Covered:**

- Introduction to the Chinese MAH System.
- MAH Legislative History.
- Administration Structure.
- Overview of MAH Responsibilities.
- Marketing Authorization Application.
- Pharmaceutical Product Import.
- Pharmaceutical Product Distribution.
- Agent of Overseas MAH.
- The Challenges &amp; Benefits of Appointing MAH Agent in China.
- Tips for Navigating the MAH Agent Landscape in China.
- Q&amp;A Session.

As a continuous practice, Freyr organizes more webinar sessions related to Regulatory aspects in Life Sciences. We presume you would like to be a part of all those sessions. If so, let us have an opportunity to inform you about our next session.



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Jane has over seventeen (17+) years of experience in new drug R&amp;D and more than twenty (20+) years in Regulatory Affairs (RA). She possesses a deep understanding of NMPA and global regulations, including FDA, EU, and ICH. Her strong scientific background, extensive knowledge, and previous role as a CDE reviewer contribute to her comprehensive understanding and interpretation of these regulations.





## Presented By

### Jane Zhang

Sr. Director Regulatory Affairs, Freyr China