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Clinical site
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#	Item
51	SOP 20B- NIH IRB RESPONSIBILITIES WHEN REVIEWING LOCAL CONTEXT Add to Reading List Source URL: ohsr.od.nih.gov Language: English - Date: 2014-03-10 08:07:30 Health Institutional review board National Institutes of Health Declaration of Helsinki Clinical site Office for Human Research Protections John E. Fogarty International Center Clinical research Research Medicine
52	Site Manager Job Description Reports to: Location: Position: Operations Manager Add to Reading List Source URL: goape.com Language: English - Date: 2014-09-26 10:45:49 Occupational safety and health Pharmacology Clinical research Pharmaceutical industry
53	IDT Site Experience - CQI Helen O’Shaughnessy Clinical Practice and Training Lead, LCW James Yates Implementation Manager, NHS Pathways Add to Reading List Source URL: systems.hscic.gov.uk Language: English Statistics Data analysis Outlier
54	SITE SELECTION BIAS IN PROGRAM EVALUATION∗ Hunt Allcott† February 13, 2015 Abstract “Site selection bias” can occur when the probability that a program is adopted or evaluated Add to Reading List Source URL: www.nyudri.org Language: English - Date: 2015-05-20 16:55:42 Knowledge Clinical research Epidemiology Evaluation methods Medical statistics Randomized controlled trial Opower Meta-analysis Clinical trial Science Statistics Design of experiments
55	SOP 20: Responsibilities when the NIH Intramural Research Program Serves as a Coordinating Center for a Multi-site Trial Add to Reading List Source URL: ohsr.od.nih.gov Language: English - Date: 2014-03-10 08:07:30 Research Health Clinical research Design of experiments Pharmacology Clinical trial NIH Intramural Research Program National Institutes of Health Nursing research Medicine
56	*** Contact On-site clinical mentoring IMCI-ETAT training course for children (optional) Add to Reading List Source URL: imaiimcialliance.org Language: English* - Date: 2012-09-12 17:35:47 Public health Dentistry Surgery Pandemics Clinical officer Infection control Flu pandemic Disease surveillance Influenza Medicine Health Epidemiology
57	Outline for Requesting Approval of a New Clinical Site Add to Reading List Source URL: www.coarc.com Language: English - Date: 2015-04-15 15:03:06 Respiratory therapy Commission on Accreditation for Respiratory Care
58	Guidance for Maintenance of an Investigator Site File The Investigator Site File should contain the essential documents that permit an evaluation of the conduct of a research project. The contents of the Site File serve Add to Reading List Source URL: www.shu.ac.uk Language: English - Date: 2014-02-04 08:25:52 Ethics Design of experiments Pharmacology Drug safety Institutional review board Research ethics Clinical trial Clinical site Clinical research Research Applied ethics
59	Executive Summary Munich, JulyFGK Representative Service GmbH announces that it has passed successfully the first inspection of a Legal Representative in the European Union by authorities. Early in 2008, FGK Repr Add to Reading List Source URL: www.fgk-rs.com Language: English - Date: 2010-10-28 18:00:00 Pharmacology Health Design of experiments Medical statistics Pharmaceutical industry Clinical trial Institutional review board Clinical site Clinical research Research Science
60	STANDARD CLINICAL TRIAL AGREEMENT __________ (“Sponsor”), a {form of entity} organized under the laws of {State} and the Board of Regents of the University of Wisconsin System (“Site”), a state-controlled higher Add to Reading List Source URL: www.rsp.wisc.edu Language: English - Date: 2015-01-06 13:40:21 Science Design of experiments Pharmacology Scientific method Clinical trial Institutional review board Case report form Investigational Device Exemption Trade secret Clinical research Research Pharmaceutical industry