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Science Review Board
Results: 2734

#	Item
231	NATIONAL NETWORK OF RESEARCH ETHIC’S COMMITTEES IN BULGARIA LEGAL BASIS Drug law Add to Reading List Source URL: www.eurecnet.org Language: English - Date: 2012-12-10 08:35:03 Scientific method Ethics Committee Institutional review board Clinical trial Good Clinical Practice Ethics Medical school Outline of ethics Medical ethics Clinical research Research Science
232	http://www.eurecnet.org/newsletter Newsletter 2014 / 01 Informed Consent and Data Protection in Multicenter Genetic-Neuroimaging Studies Add to Reading List Source URL: www.eurecnet.org Language: English - Date: 2014-11-13 05:14:24 Science Clinical research Research ethics Biological databases Biobanks Biobank Informed consent Institutional review board Human subject research Ethics Medical ethics Applied ethics
233	RECs system in Latvia Vents Silis (Riga Stradins University) Rinalds Mucins (Central Medical Ethics Committee) EURECNET conference Bratislava, 12-13 April, 2012 Add to Reading List Source URL: www.eurecnet.org Language: English - Date: 2012-12-10 08:35:11 Health Ethics Committee Clinical trial Institutional review board Good Clinical Practice Medical ethics Medical research Clinical research Research Science
234	DOC Document Add to Reading List Source URL: www.dlr.de Language: English - Date: 2015-04-14 08:50:35 Information Pharmaceutical industry Design of experiments Pharmacology Evaluation methods Clinical trial Institutional review board Patient recruitment Statistics Research Science Clinical research
235	PHR Research Funding Board – Decisions from theJune 2013 meeting Full proposals The Research Funding Board recommended the following full proposals for either immediate funding or for funding subject to certain Add to Reading List Source URL: www.nets.nihr.ac.uk Language: English - Date: 2014-03-24 12:08:53 Design of experiments Science Health promotion Addiction Intervention Randomized controlled trial Cluster randomised controlled trial Systematic review Violence Health Medicine Clinical research
236	DANA-FARBER / HARVARD CANCER CENTER STANDARD OPERATING PROCEDURES FOR HUMAN SUBJECT RESEARCH TITLE: Data and Safety Monitoring Committee (DSMC) Data Submission Compliance SOP #: DATA-104 (formerly QA-724) Page: 1 of 4 Add to Reading List Source URL: www.dfhcc.harvard.edu Language: English - Date: 2014-02-20 14:53:12 Design of experiments Pharmacology Food and Drug Administration Medicine Drug safety Clinical trial Institutional review board Protocol Investigational New Drug Clinical research Science Research
237	DF/HCC Practice Differences in Comparison to ICH GCP Guidelines 1. INTRODUCTORY STATEMENT: Dana-Farber/Harvard Cancer Center (DF/HCC) follows the International Conference on Harmonisation Guidelines for Good Clinical Pra Add to Reading List Source URL: www.dfhcc.harvard.edu Language: English - Date: 2012-07-03 16:02:31 Pharmaceutical industry Scientific method Design of experiments Pharmacology Medical ethics Institutional review board Clinical trial Good Clinical Practice Declaration of Helsinki Clinical research Research Science
238	Info Sheet - Operations Office for Human Research Studies Guidance on Central IRB Review Process The DFCI IRB has made specific arrangements for use of the following Central IRBs for review of DF/HCC conducted research: Add to Reading List Source URL: www.dfhcc.harvard.edu Language: English - Date: 2015-03-26 15:48:26 Science Design of experiments Pharmacology Pharmaceutical sciences Food and Drug Administration Clinical trial Adverse event Institutional review board Clinical research Pharmaceutical industry Research
239	IRB Project Number (Obtain from IRB Approval Letter) __ __ __ - __ __ PRIVATE Add to Reading List Source URL: www.njit.edu Language: English - Date: 2015-01-29 16:57:40 Science Scientific method Design of experiments Pharmacology Drug safety Institutional review board Adverse event Clinical research coordinator Clinical trial Clinical research Research Pharmaceutical industry
240	Info Sheet - Operations Office for Human Research Studies Guidance on Central IRB Review Process The DFCI IRB has made specific arrangements for use of the following Central IRBs for review of DF/HCC conducted research: Add to Reading List Source URL: www.dfhcc.harvard.edu Language: English - Date: 2015-03-26 15:48:38 Science Design of experiments Pharmacology Pharmaceutical sciences Food and Drug Administration Clinical trial Adverse event Institutional review board Clinical research Pharmaceutical industry Research

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