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Clinical research
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#	Item
221	New NIH guidelines to improve Experimental Rigor and Reproducibility Oswald Steward Professor, Department of Anatomy & Neurobiology Senior Associate Dean for Research University of California School of Medicine Add to Reading List Source URL: som.uci.edu Language: English - Date: 2016-05-23 22:05:56 Health Medical research Drug discovery Pharmaceutical industry Nursing research Scientific method Measurement Reproducibility Amyotrophic lateral sclerosis National Institute of Neurological Disorders and Stroke Clinical trial Pre-clinical development
222	Comments of the German Medical Association To the Consultation Paper of the European Commission ofon the ‘Clinical Trials Directive’ EC Add to Reading List Source URL: www.bundesaerztekammer.de Language: English - Date: 2014-10-01 03:07:02 Medical research Clinical research Research Medical ethics Clinical research ethics Pharmaceuticals policy Design of experiments Clinical Trials Directive Ethics committee Clinical trial Institutional review board Informed consent
223	A Video Game Improves Behavioral Outcomes in Adolescents and Young Adults With Cancer: A Randomized Trial Add to Reading List Source URL: www.hopelab.org Language: English - Date: 2016-04-06 14:44:41 Health Medical research Clinical research Clinical pharmacology Medical statistics Clinical trials Medical terminology HopeLab Compliance Re-Mission Clinical endpoint Adherence management coaching
224	A Blueprint for Health Records Research in Scotland APPENDIX 2 MEMBERSHIP OF SHIP Principal Investigator: Prof Add to Reading List Source URL: www.scot-ship.ac.uk Language: English - Date: 2014-04-01 08:15:20 Scotland Universities in Scotland University of Glasgow Universities in the United Kingdom United Kingdom University of Dundee Robertson Centre for Biostatistics Glasgow Clinical Research Facility Glasgow Clinical Trials Unit University of St Andrews NHS Scotland University of Edinburgh
225	CONSORTIUM OF FOOD ALLERGY RESEARCH STATISTICAL AND CLINICAL COORDINATING CENTER CoFAR COLLABORATIVE RESEARCH PROJECT APPLICATION Add to Reading List Source URL: web.emmes.com - Date: 2012-03-16 12:13:11
226	Release Notes for Harmonised Technical Guidance for eCTD Submissions in the EU v3.0 This document highlights the changes incorporated in version 3.0, in comparison with version 2.0, of the eCTD guidance document. For cle Add to Reading List Source URL: esubmission.ema.europa.eu Language: English - Date: 2016-08-19 03:16:10 Medical research Clinical research Health Clinical data management Computing Electronic common technical document Pharmaceutical industry Pharmaceuticals policy Marketing authorization Section Diff utility Drug Master File
227	REVIEWING THE ETHICAL REVIEWERS: THE SIDCER/FERCAP EXPERIENCE* Lisa Hamadian, M.D. & Allan K. Johansen, D.V.M. Despite playing a key role in a clinical trial, the ethics committee (EC) is an entity over which sponsor aud Add to Reading List Source URL: www.fercap-sidcer.org Language: English - Date: 2012-02-08 01:30:03 Ethics Medical research Applied ethics Medical ethics Clinical research ethics Research ethics Social research Ethics committee Institutional review board Human subject research
228	Evidence Based Medicine Basic terms Add to Reading List Source URL: ubi.lf1.cuni.cz Language: English - Date: 2016-03-30 06:17:35 Statistics Health Design of experiments Hypothesis testing Medical statistics Clinical research Epidemiology Evidence-based medicine Cohort study Null hypothesis Randomized controlled trial Number needed to treat
229	Emergency Use: means the use of a test article on a human subject in a life-threatening situation in Add to Reading List Source URL: humansubjects.stanford.edu Language: English - Date: 2016-04-12 01:21:50 Medical research Health Food and Drug Administration Pharmaceutical industry Drug safety Clinical pharmacology Expanded access Clinical trial Investigational New Drug Informed consent New drug application Health Insurance Portability and Accountability Act
230	1 AugustElectronic Application Forms are now fully available for use For initial marketing authorisation (human and veterinary), variation and renewal applications Add to Reading List Source URL: esubmission.ema.europa.eu Language: English - Date: 2016-08-19 03:15:40 Pharmaceuticals policy Health Medical research Clinical data management Clinical research Pharmaceutical industry European Union EudraLex European Medicines Agency Electronic common technical document Common Technical Document Marketing authorization

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