Abstract: This paper discussed the method about how to administrate and innovate the ethics comittees(EC) documents during the process of clinical research. By setting up the regulations of document administration, elevate the idea of EC secretary, and improve the level of EC document administration. By these method, we can truly show the process of EC review, ensure EC protecting the rights of subjects and provide the scientific, truly, accurate, integrated, credible evidence of clinical research.

Key words: ethics committee, document administration, clinical research