Register for Upcoming Webinar on DEC. 8 @ 11AM

China Green Pathways: Expedite your Market Entry in China

2025 China NMPA Bluebook is here:

Download Your Copy Today

[wpml_language_selector_widget]

China 1.2 Billion registered cell phone users: CFDA Mobile Medical Device Technical Review Guideline Announced

January 30, 2018

Share:

CFDA is regulating mobile medical devices even closer. On 29 Dec, 2017, Guideline for Technical Review of Mobile Medical Device Registration issued by CFDA, specifying the data preparing for registration to applicants and providing reference for technical review departments.

Have Questions?

Related Services

Resources

NMPA (CFDA) Regulations

NMPA (CFDA) Newsletters

Recorded Webinars

White Papers

Brochures

Recent Events

RAPS Webcast: 2023 NMPA (CFDA) Key Updates and Look Ahead on 2024

Medical Device Made-in-China Policy: A Comprehensive Review and Implementation

Related Posts

China NMPA Delayed UDI Implementation Date to Jan 1st, 2021

NMPA issued a notice today to delay the UDI implementation

China’s NMPA UDI Database Filing and Mandatory Fields for New Rules

Last year, NMPA issued a number of UDI related policies

CMD New Webinar! Learn China Mandatory Period Risk Evaluation Report (PRER) and the latest PMS Requirements in China NMPA and US FDA

Thursday, July 9, 2020 | 12:00 pm – 1:10 pm

NMPA Roundup February Coronavirus Special Issue

Amid the novel Coronavirus (COVID-19) outbreak, we deliver the Coronavirus

Practical Lessons for Coronavirus Related Products Fast Track Clearance in China

Wednesday, March 18, 2020 | 12:00 pm – 12:45 pm ETIn

Coronavirus Spurs Emergency Device Approvals in China; Reveals Lessons for Manufactures to Speed Market Entry (I)

While the Novel Coronavirus (COVID-19) has caused a tragic loss

Read More: Uncategorized

Search

Get Updated

Receive Updates in Your Inbox

Categories

Archives