Is it a good news that the medical device testing fees would be eliminated in China?

All the medical devices require local testing in China for CFDA registration, which is generally done in a CFDA-accredited lab. Recently, the Ministry of Finance of China has released a notice to eliminate several items of fees charged by the authorities (Finance Tax [2017] No. 20), including the certification fees for drug good manufacturing practice (GMP) and drug Good Supply Practice (GSP), as well as the testing fees for both drugs and medical devices. This notice became effective since April 1st, 2017.

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CFDA is planning to down-size the number of categories for medical devices

The China Food and Drug Administration (CFDA) has been using the four-digits category system for medical device since the year of 2000. Currently, all medical devices are divided into 43 categories from “6801” to “68xx”. The category information is embedded in the CFDA certification number as the second and third digits. For example, a certificate of 2016-3642017 shows the product is in the category of 6864 Medical sanitation material and dressing.

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2015-10-27 Webinar OSMUNDA Will Reveal the Secrets of Medical Device Approval in China in the MEDICAL DEVICE REGULATORY UPDATE Webinar

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Neque porro quisquam est qui dolorem iipsum se quia dolor sit amet, consectetur, adipiscism velittes.There is no one who loves pain itself, who seeks after it and wants to have it, simply because it is pain.

Lorem Ipsum is simply dummy text of the printing and typesetting industry. Lorem Ipsum has been the industry’s standard dummy text ever since the 1500s, when an unknown printer took a galley of type and scrambled it to make a type specimen book. It has survived not only five centuries.

中国:指南GMP审核

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和任何一个谁不是自己,他Iipsum痛悲坐阿梅德,consectetur,adipiscism velittes.There没有一个谁爱的痛苦本身,之后谁搞,想拥有它,只是因为它是痛苦。

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