<tt id="6hsgl"><pre id="6hsgl"><pre id="6hsgl"></pre></pre></tt>
          <nav id="6hsgl"><th id="6hsgl"></th></nav>
          国产免费网站看v片元遮挡,一亚洲一区二区中文字幕,波多野结衣一区二区免费视频,天天色综网,久久综合给合久久狠狠狠,男人的天堂av一二三区,午夜福利看片在线观看,亚洲中文字幕在线无码一区二区
          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: 99在线视频免费观看| 午夜AAAAA级岛国福利在线| 孕交videos小孕妇xx| 在线 欧美 中文 亚洲 精品| 欧美精品1区2区| 老司机免费的精品视频| 日韩亚洲AV无码一区二区不卡| 久久国产亚洲一区二区三区| 97久久精品人人做人人爽| 国产乱人伦真实精品视频| 日韩精品视频一区二区不卡| 日韩精品中文字幕人妻| 国产精品 欧美 亚洲 制服| 欧美黑人XXXX性高清版| 粉嫩少妇内射浓精videos| 99在线视频免费观看| 狠狠亚洲超碰狼人久久| 日本中文字幕乱码免费| 成人深夜福利av在线| 九九热精品视频在线| 亚洲欧美精品综合一区| 97精品伊人久久久大香线蕉| 一区二区在线观看成人午夜| 99热成人精品热久久66| 狠狠精品干练久久久无码中文字幕| 激情五月日韩中文字幕| 国产熟女肥臀精品国产馆乱| 大桥未久亚洲无av码在线| 色天天综合网| 超碰伊人久久大香线蕉综合| 国产综合久久久久久鬼色| 天堂www在线中文| 乱人伦人妻系列| (原创)露脸自拍[62p]| 久久亚洲av综合悠悠色| 成 人免费va视频| 99偷拍视频精品一区二区| 性人久久久久| 蜜臀视频在线观看一区二区| 亚洲国产中文字幕精品| 精品视频不卡免费观看|