Assessing data quality and the variability of source data verification auditing methods in clinical research settings
暂无分享,去创建一个
[1] Michael G. Kahn,et al. Remote Source Document Verification in Two National Clinical Trials Networks: A Pilot Study , 2013, PloS one.
[2] J D Horbar,et al. An assessment of data quality in the Vermont-Oxford Trials Network database. , 1995, Controlled clinical trials.
[3] J. Higgins,et al. Cochrane Handbook for Systematic Reviews of Interventions , 2010, International Coaching Psychology Review.
[4] Gordon B. Davis,et al. User Acceptance of Information Technology: Toward a Unified View , 2003, MIS Q..
[5] Arun Bhatt. Quality of clinical trials: A moving target , 2011, Perspectives in clinical research.
[6] D. Moher,et al. Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement , 2009, BMJ.
[7] C. Reid,et al. Quality control activities associated with registries in interventional cardiology and surgery. , 2011, Heart, lung & circulation.
[8] Chitra Bargaje. Good documentation practice in clinical research , 2011, Perspectives in clinical research.
[9] R. Califf,et al. Developing systems for cost-effective auditing of clinical trials. , 1997, Controlled clinical trials.
[10] S L George,et al. Guidelines for quality assurance in multicenter trials: a position paper. , 1998, Controlled clinical trials.
[11] Sheena McCormack,et al. The potential for central monitoring techniques to replace on-site monitoring: findings from an international multi-centre clinical trial , 2012, Clinical trials.
[12] Jules Mitchel,et al. Risk-Based Source Data Verification Approaches: Pros and Cons , 2010 .
[13] M. Mack,et al. Are unaudited records from an outcomes registry database accurate? , 2004, The Annals of thoracic surgery.
[14] Carl F. Pieper,et al. Quantifying Data Quality for Clinical Trials Using Electronic Data Capture , 2008, PloS one.
[15] Jane M Blazeby,et al. A systematic review of on-site monitoring methods for health-care randomised controlled trials , 2013, Clinical trials.
[16] Catrin Tudur Smith,et al. The Value of Source Data Verification in a Cancer Clinical Trial , 2012, PloS one.
[17] Roxanne E. Ward,et al. Examining Methods and Practices of Source Data Verification in Canadian Critical Care Randomized Controlled Trials , 2013 .
[18] K. Mate,et al. Improving public health information: a data quality intervention in KwaZulu-Natal, South Africa. , 2012, Bulletin of the World Health Organization.
[19] Daniel R. Masys,et al. Measuring the Quality of Observational Study Data in an International HIV Research Network , 2012, PloS one.
[20] J. van den Broeck,et al. Maintaining data integrity in a rural clinical trial , 2007, Clinical trials.
[21] 药学. International Conference on Harmonisation of Technical Requirements , 2013 .
[22] Meredith Nahm,et al. What can we learn from a decade of database audits? The Duke Clinical Research Institute experience, 1997—2006 , 2009, Clinical trials.
[23] Sylvie Chevret,et al. Validation of a risk-assessment scale and a risk-adapted monitoring plan for academic clinical research studies--the Pre-Optimon study. , 2011, Contemporary clinical trials.
[24] Ichael,et al. THE NATIONAL CANCER INSTITUTE AUDIT OF THE NATIONAL SURGICAL ADJUVANT , 2000 .
[25] Charles Safran,et al. Toward a national framework for the secondary use of health data: an American Medical Informatics Association White Paper. , 2007, Journal of the American Medical Informatics Association : JAMIA.
[26] Sue E Bowman. Impact of electronic health record systems on information integrity: quality and safety implications. , 2013, Perspectives in health information management.
[27] D. Moher,et al. Preferred Reporting Items for Systematic Reviews and Meta-Analyses: The PRISMA Statement , 2009, BMJ : British Medical Journal.
[28] D. Sarfati,et al. An audit of colon cancer data on the New Zealand Cancer Registry. , 2008, The New Zealand medical journal.
[29] Barbara Castelnuovo,et al. Implementation of Provider-Based Electronic Medical Records and Improvement of the Quality of Data in a Large HIV Program in Sub-Saharan Africa , 2012, PloS one.
[30] E van der Schueren,et al. Quality control of validity of data collected in clinical trials. EORTC Study Group on Data Management (SGDM). , 1989, European journal of cancer & clinical oncology.
[31] Jonathan R Davis,et al. Assuring Data Quality and Validity in Clinical Trials for Regulatory Decision Making , 1999 .
[32] Eric E. Smith,et al. Data quality in the American Heart Association Get With The Guidelines-Stroke (GWTG-Stroke): results from a national data validation audit. , 2012, American heart journal.
[33] Christian Ohmann,et al. Risk analysis and risk adapted on-site monitoring in noncommercial clinical trials , 2009, Clinical trials.
[34] Samantha J. Togni,et al. Understanding uptake of continuous quality improvement in Indigenous primary health care: lessons from a multi-site case study of the Audit and Best Practice for Chronic Disease project , 2010, Implementation science : IS.
[35] R. Franklin,et al. Verification of data in congenital cardiac surgery , 2008, Cardiology in the Young.
[36] Jessica D. Tenenbaum,et al. Practices and perspectives on building integrated data repositories: results from a 2010 CTSA survey , 2012, J. Am. Medical Informatics Assoc..
[37] Dirk Hasenclever,et al. Risk-adapted monitoring is not inferior to extensive on-site monitoring: Results of the ADAMON cluster-randomised study , 2017, Clinical trials.
[38] Eric L Eisenstein,et al. Reducing the costs of phase III cardiovascular clinical trials. , 2005, American heart journal.