China Med Device - Accelerate Your Medical Device's Entry Into China
China Med Device (CMD) has brought a great deal of knowledge and understanding to our team to help us navigate the complexities of bringing a product to market in China. Specifically we have gained a …
China Medical Device - 加速您的医疗器械进入中国
China Med Device (CMD) has brought a great deal of knowledge and understanding to our team to help us navigate the complexities of bringing a product to market in China. Specifically we have gained a …
Suspension of Importation to China by NMPA - China Med Device
Jun 27, 2019 · In 2019, NMPA (CFDA) has announced 3 batches of Overseas Inspection Results. A total of 24 foreign manufacturers, including Medtronic, Becton Dickinson, Boston Scientific, B.Brown, …
CFDA Updates: China Joins ICH - China Med Device
“CFDA’s joining ICH is a historic event that marks an important milestone where China’s drug and medical device industry is going to further open to the world.”, commented by Mr Lin YUAN, CDFA’s …
Blogs - Page 58 of 73 - China Med Device
Weekly CFDA News Roundup covers policies, regulations, QA/recall/AE, and new approvals in medical device and IVD in China. It is edited by China Med Device, LLC, a consulting firm specializing Read …
Blogs - Page 48 of 74 - China Med Device
Daily updates for China medtech market assessment, CFDA regulation, China funding oppotunies.
Blogs - Page 45 of 69 - China Med Device
Dec 16, 2019 · Monthly CFDA News Roundup covers government announcement, policies, standards, guidelines, QA/recall/AE, and new approvals in medical device and IVD in China. It is edited by …
202109 NMPA (CFDA) Newsletter - China Med Device
Download Resource Package: September 2021 NMPA (formerly known as CFDA) Newsletter with all the latest information on medical device news...
CFDA announced the new "Medical Device Classification Catalogue"
Sep 7, 2017 · On August 31, CFDA announced the new “Medical Device Classification Catalogue”. This new catalogue will be implemented on August 1 ST, 2018. The revised medical device classification …
Further Reform Registration Reviewing and Approval Guidelines
Nov 17, 2017 · 6) Improve policy implementation In 2015, the State Council started the reform releasing guidelines for reform registration reviewing and approval of medical devices/drugs. From 2015 to …