www射-国产免费一级-欧美福利-亚洲成人福利-成人一区在线观看-亚州成人

USEUROPEAFRICAASIA 中文雙語Fran?ais
China
Home / China / Society

Backlog in drug approvals reduced

By Shan Juan | China Daily | Updated: 2016-12-20 07:14

The backlog of drug registration cases in China has been substantially reduced, with 9,000 applications awaiting approval, compared with a peak of 22,000 last year, a senior official said.

"Reforms are underway to speed up the drug evaluation and registration process to improve public access to advanced treatments," said Li Jinju, deputy director of the China Food and Drug Administration's drug and cosmetics registration department.

"But safety and quality will never be compromised," Li said.

Backlog in drug approvals reduced

A shortage of staff in drug evaluation and registration is mainly to blame, she said. "That was addressed by the reforms."

There are about 10,000 applications for drug registration per year.

Before 2015, the administration's drug evaluation center had only 130 staff, including 80 specializing in drug evaluation, Li said. In comparison, a similar department in the United States has 5,000, and in Japan there are 700.

Under the reforms, "we hired more, but it takes time to build capacity and train staff as the evaluation work is highly demanding technically", she said.

The strain is expected to be substantially relieved in two to three years, she estimated.

Also, new drugs in urgent and high demand clinically will be fast-tracked for approval, she added.

So far, 146 candidates have been fast-tracked for registration and approval, including the HPV vaccine, which protects women from cervical cancer caused by HPV infection and was submitted for approval about 10 years ago.

To enhance efficiency, other reform measures like strengthened communication with drug developers and streamlined interior working procedures were introduced as well after March, she said.

In March, Bi Jingquan, head of the administration, first pledged reforms of drug registration to beef up efficiency.

He recognized that the process took longer in China and that "there was a backlog of cases".

In China, a drug candidate needs to go through applications, three phases of clinical trials, and registration and approval to become available for patients, a process that can take years.

shanjuan@chinadaily.com.cn

Editor's picks
Copyright 1995 - . All rights reserved. The content (including but not limited to text, photo, multimedia information, etc) published in this site belongs to China Daily Information Co (CDIC). Without written authorization from CDIC, such content shall not be republished or used in any form. Note: Browsers with 1024*768 or higher resolution are suggested for this site.
License for publishing multimedia online 0108263

Registration Number: 130349
FOLLOW US
 
主站蜘蛛池模板: 久久成人综合网 | www国产精品| 福利一二三区 | 欧美激情成人网 | 欧美色xxxx| 精品久久久久国产 | 99精品小视频 | 国产精品一级视频 | 亚洲三级网址 | 一区视频在线播放 | 精品视频99 | 亚洲另类视频 | 青青青青爽视频在线播放 | 中午字幕在线观看 | jiz欧美高清| 欧美大片在线观看成人 | 成人av手机在线观看 | 精品久久久日韩精品成人 | 欧美特黄一级高清免费的香蕉 | 91精品国产福利尤物免费 | 在线观看中文字幕亚洲 | 国产视频精品久久 | 国产精品久久久久久久久岛 | 亚洲男人的性天堂 | 99视频国产精品 | 一级全黄视频 | 曰批美女免费视频播放 | 成人免费网站在线观看 | 欧美成人性色生活片免费在线观看 | 欧美成人aaaa免费高清 | 久久99热成人精品国产 | 成人合集大片bd高清在线观看 | 国产在线精品一区二区高清不卡 | 精品国产高清a毛片无毒不卡 | 亚洲素人在线 | 特黄特黄aaaa级毛片免费看 | 久久欧美精品 | 亚洲国产一区二区三区四区五区 | 高清波多野结衣一区二区三区 | 成人精品视频在线观看播放 | 久久青草免费线观最新 |