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The REWARD (REduce research Waste And Reward Diligence)Statement

We recognize that despite our commitment to excellence in research, much remains to be done to reduce research waste and improve the value of our contributions. We will maximize our research potential in the following areas:

  1. We determine the right research focus;
  2. We use reliable research design, implementation and analysis;
  3. Supervision and management are directly proportional to risk;
  4. All information on the methodology and results of the study is accessible;
  5. The research report is complete and available.


We have the responsibility not only to study, but also to promote the development of knowledge. This will help to improve the health and lives of all people everywhere. As funders, regulators, businesses, publishers, editors, researchers, research users and others - we are committed to playing a role in increasing the value of research and reducing research waste.

Notice of contribution to the 4th International Conference on clinical trial methodology and the 38th annual meeting of clinical trial Association (as of November 10)

The Fourth International Conference on clinical trial methodology and the 38th annual meeting of clinical trial Association will be held in May 2017 in Liverpool, UK. This is the first annual meeting of clinical trial Association, jointly held with the International Conference on clinical trial methodology, which will bring together international peers in the field of clinical trial work, including clinical trial design experts, methodology experts, doctors and specialists It will provide a larger international platform for clinical trial personnel to cooperate and discuss new ideas. This conference includes three keynote speeches and a series of symposiums. The keynote speech will be arranged from May 7 to 10, 2017, and the symposium will be arranged on May 6, 2017 (Sunday). We hope you will pay attention to and actively contribute to the conference (the abstract submission deadline is November 10, 2016). Please refer to  。

Technical guidelines for clinical trial data management

The quality of clinical trial data is the basis of evaluating clinical trial results. In order to ensure the accuracy, reliability and scientific credibility of clinical trial results, a series of regulations, regulations and guiding principles have been issued by the international community and countries around the world to standardize the whole process of clinical trial data management. At the same time, the development of modern clinical trials of new drugs and the continuous progress of science and technology, especially the development of computers and networks, provide new technical support for the standardization of clinical trials and data management, and also promote the governments of various countries and the international community to actively explore new standardized models of clinical trials and data management.

Guiding principles of electronic data acquisition technology in clinical trials

In recent years, with the rapid development of electronic data collection and data entry in clinical trials, more and more countries have adopted electronic data collection and paper-based data collection methods to improve the quality of clinical trials Sub data acquisition technology to ensure data quality.

In order to promote the integrity, accuracy, authenticity and reliability of electronic data in clinical trials in China, it is necessary to clearly explain the basic considerations and principles for the application of electronic data acquisition technology in clinical trials The purpose of this paper is to help and guide the relevant parties, including the sponsor, cro and clinical researchers, to standardize and reasonably apply EDI technology in clinical trials.

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