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Clinical study design
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521	Counseling Potential Participants About a Clinical Trial If you are counseling a potential study participant about a clinical trial, the following questions are a convenient way of organizing the information you want to Add to Reading List Source URL: www.fxbcenter.org Language: English - Date: 2007-11-12 09:29:35 Medicine Pharmacology Design of experiments Evaluation methods Medical ethics Clinical trial Alternative medicine Placebo Randomized controlled trial Clinical research Research Science
522	RMT-IRB PI Check-list for Study Closeout Study Closeout Checklist Use this form to close out any RMT-IRB-approved study. Submit this completed form within 30 days of completion or termination of all research activity for Add to Reading List Source URL: mtwytlc.org Language: English - Date: 2011-07-11 16:15:20 Research Design of experiments Pharmacology Drug safety Closeout Clinical research Pharmaceutical industry
523	Clinical Trials What is a clinical trial? A clinical trial is a research study involving people who volunteer to participate. Clinical trials evaluate whether a new drug, treatment, or combination of treatments is safe, Add to Reading List Source URL: www.cancer.net Language: English - Date: 2014-04-14 15:59:31 Health Pharmaceutical industry Food and Drug Administration Design of experiments Pharmacology Clinical trial American Society of Clinical Oncology Investigational New Drug Data monitoring committees Clinical research Research Medicine
524	Recommendations from the Clinical Trials Task Force (CTD-TF) as regards Phase II trials Phase II trials evaluate the activity, and toxicity, of a new agent either as monotherapy or in combination. Trial designs with a s Add to Reading List Source URL: ctep.cancer.gov Language: English - Date: 2010-07-08 21:03:14 Science Epidemiology Design of experiments Pharmacology Medical statistics Biomarker Crossover study Randomized controlled trial Clinical trial Medicine Clinical research Research
525	An Introduction to Causal Analysis on Observational Data using Propensity Scores Margie Rosenberg, PhD, FSA Brian Hartman, PhD, ASA Shannon Lane University of Wisconsin – Madison Add to Reading List Source URL: umanitoba.ca Language: English* - Date: 2014-08-19 17:08:39 Propensity score Rubin causal model Observational study Causality Clinical trial University of Wisconsin–Madison Confounding Statistics Science Design of experiments
526	Food and Drug Administration Rockville MD[removed]I .... . Add to Reading List Source URL: www.fda.gov Language: English - Date: 2000-09-25 04:40:55 Science Clinical research Design of experiments Evaluation methods Bioethics Food and Drug Administration Placebo-controlled study Clinical trial Antidepressant Pharmacology Medicine Research
527	INDIANA UNIVERSITY SOUTHEAST INSTITUTIONAL REVIEW BOARD (IRB) REVIEW REQUEST FORM FOR THE INCLUSION OF PRISONERS IN RESEARCH Principal Investigator: IRB Study: Add to Reading List Source URL: www.ius.edu Language: English - Date: 2009-01-12 09:20:28 Applied ethics Criminal law Medical ethics Design of experiments Pharmacology Institutional review board Human subject research Prison Parole Ethics Clinical research Research
528	Federal Register / Vol. 64, No[removed]Friday, September 24, [removed]Notices 49. Port Gamble S’Klallam Reservation in Kitsap County in Washington ($285,000) Add to Reading List Source URL: www.fda.gov Language: English - Date: 1999-09-24 01:39:00 Scientific method Pharmacology Design of experiments Pharmaceutical industry Evaluation methods Assay sensitivity Placebo-controlled study Clinical trial Placebo Clinical research Science Research
529	2011 Mental Health Surveillance Study: Design and Estimation Report (External) Add to Reading List Source URL: www.samhsa.gov Language: English - Date: 2013-02-22 09:55:02 Mental health Sample size determination Survey methodology RTI International Stratified sampling Mental disorder Severe combined immunodeficiency Statistics Sampling Structured Clinical Interview for DSM-IV
530	INDIANA UNIVERSITY SOUTHEAST INSTITUTIONAL REVIEW BOARD (IRB) REVIEW DOCUMENTATION OF REVIEW AND APPROVAL (DRA) IU Southeast IRB STUDY NUMBER:______________ (IRB Office will assign) Add to Reading List Source URL: www.ius.edu Language: English - Date: 2010-09-01 10:59:59 Science Design of experiments Pharmacology Scientific method Drug safety Institutional review board Informed consent Clinical research coordinator Clinical trial Clinical research Research Medical ethics