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Works citing "The Use of Electronic Data Capture Tools in Clinical Trials: Web-Survey of 259 Canadian Trials"

Khaled El Emam, Elizabeth Jonker, Margaret Sampson, Karmela Krleža-Jerić, Angelica Neisa
J Med Internet Res 2009 (Mar 09); 11(1):e8 

According to Crossref, the following articles are citing this article (DOI 10.2196/jmir.1120):

(note that this is only a small subset of citations)

 
1. Zhang Y, Sun W, Gutchell EM, Kvecher L, Kohr J, Bekhash A, Shriver CD, Liebman MN, Mural RJ, Hu H. QAIT: A quality assurance issue tracking tool to facilitate the improvement of clinical data quality. Computer Methods and Programs in Biomedicine 2013;109(1):86 [CrossRef]
 
2. Nesbitt G, McKenna K, Mays V, Carpenter A, Miller K, Williams M. The Epilepsy Phenome/Genome Project (EPGP) informatics platform. International Journal of Medical Informatics 2013;82(4):248 [CrossRef]
 
3. van Valkenhoef G, Tervonen T, Zwinkels T, de Brock B, Hillege H. ADDIS: A decision support system for evidence-based medicine. Decision Support Systems 2012; [CrossRef]
 
4. Allison M. Reinventing clinical trials. Nature Biotechnology 2012;30(1):41 [CrossRef]
 
5. Valkenhoef G, Tervonen T, Brock B, Hillege H. Deficiencies in the transfer and availability of clinical trials evidence: a review of existing systems and standards. BMC Medical Informatics and Decision Making 2012;12(1):95 [CrossRef]
 
6. El Emam K, Moreau K, Jonker E. How Strong are Passwords Used to Protect Personal Health Information in Clinical Trials?. Journal of Medical Internet Research 2011;13(1):e18 [CrossRef]
 
7. Eysenbach G. CONSORT-EHEALTH: Improving and Standardizing Evaluation Reports of Web-based and Mobile Health Interventions. Journal of Medical Internet Research 2011;13(4):e126 [CrossRef]
 
8. Herzberg S, Rahbar K, Stegger L, Schäfers M, Dugas M. Concept and implementation of a computer-based reminder system to increase completeness in clinical documentation. International Journal of Medical Informatics 2011;80(5):351 [CrossRef]
 
9. Porzsolt F. Von der Studienplanung bis zur Nutzenbewertung: Mit oder ohne pharmazeutische Industrie?. Medizinische Klinik 2010;105(12):930 [CrossRef]
 
10. Lu Z. Technical challenges in designing post-marketing eCRFs to address clinical safety and pharmacovigilance needs. Contemporary Clinical Trials 2010;31(1):108 [CrossRef]