Abstract
Data collection is an integral part of a clinical trial. The data collection process should be understood by those involved in collecting data. This understanding as well as recording of all study-related details will help to prevent the compromise of study validity.
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References
Robertson LB: Clinical trial data collection. In Current Cancer Therapeutics, edn 3. Philadelphia: Current Medicine; 1998: 437–438.
National Cancer Institute website: Investigator’s Handbook: Appendix. XII. Guidelines for reporting adverse drug reaction. Available at: http://www.ctep.info.nih.gov/handbook/HandBook Text/Appendix_XII.htm. Updated November 14, 2000.
James K, Eisenhower E, Christian M, et al.: Measuring response in solid tumors: unidimensional versus bidimensional measurement.J Natl Cancer Inst 1999, 91:523–528
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Robertson, L.B. (2001). Clinical Trials: Monitoring and Reporting of Toxicities, and Evaluating Tumor Response. In: Current Cancer Therapeutics. Current Medicine Group, London. https://doi.org/10.1007/978-1-4613-1099-0_33
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DOI: https://doi.org/10.1007/978-1-4613-1099-0_33
Publisher Name: Current Medicine Group, London
Print ISBN: 978-1-57340-176-0
Online ISBN: 978-1-4613-1099-0
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