综合一区欧美国产,99国产麻豆免费精品,九九精品黄色录像,亚洲激情青青草,久久亚洲熟妇熟,中文字幕av在线播放,国产一区二区卡,九九久久国产精品,久久精品视频免费

USEUROPEAFRICAASIA 中文雙語(yǔ)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
 
曲靖市| 当阳市| 崇文区| 滦南县| 崇州市| 景洪市| 怀化市| 西华县| 微山县| 秦皇岛市| 辽阳县| 嘉峪关市| 阿巴嘎旗| 奎屯市| 滦平县| 教育| 宁波市| 安顺市| 沛县| 秀山| 怀宁县| 诸城市| 邻水| 疏勒县| 内黄县| 武川县| 伊春市| 广水市| 红原县| 桓仁| 瓦房店市| 怀仁县| 阿克苏市| 清水河县| 托克托县| 东光县| 四川省| 大石桥市| 长宁县| 莱西市| 镇江市|