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Chinese Journal of Clinical Pharmacology and Therapeutics ›› 2004, Vol. 9 ›› Issue (5): 595-597.

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Technical procedure for design and development of clinical trial data collecting and reporting documents

WANG Yi-Bing, XIONG Ning-Ning, BO Qing-Yan, ZHOU Jian-Dong, JIANG Meng, LIU Fang, FU Wei-Min   

  1. National Base for Drug Clinical Trial, Affiliated Hospital of Nanjing University of Traditional Chinese Medicine, Nanjing,210029, J iangsu, China
  • Received:2003-12-02 Revised:2004-01-30 Published:2020-11-22

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Abstract: The quality and integrity of the clinical trial data rely importantly on the design and compilation of report documents and the collection of trial data.Therefore, based on practical experiences and with reference to the Good Clinical Data Management, we develop this technical procedure, including designing and printing procedures.

Key words: data record, data collecting, source document, case report form (CRF), technical procedure

CLC Number: