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Adverse event
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81	NSABP Foundation Inc. Department of Site and Study Management (DSSM) Research Nurse Specialist The responsibility of this position is to provide clinical expertise when appropriate to both DSSM staff and DSSM member inst Add to Reading List Source URL: www.nsabp.pitt.edu Language: English - Date: 2015-01-22 14:40:05 Pharmaceutics Science Pharmacology Medical statistics Design of experiments Clinical trial Adverse event Clinical research coordinator Clinical research Pharmaceutical industry Research
82	Documents To Be Submitted for Continuing Review The documents required for continuing review have been separated into two groups below. Group 1 includes a list of documents that all studies, regardless of review type, mu Add to Reading List Source URL: gcrc.ucdenver.edu Language: English - Date: 2015-03-10 08:39:10 Medical ethics Research Data privacy Health Insurance Portability and Accountability Act Privacy law Informed consent Adverse event Consent Pharmaceutical sciences Clinical research Pharmaceutical industry Law
83	UCSF Human Research Protection Program Add to Reading List Source URL: www.research.ucsf.edu Language: English - Date: 2015-02-26 19:59:49 Pharmaceutical industry Research Adverse event Food and Drug Administration Pharmaceutical sciences Pharmacology Clinical research
84	Safety Action Notice Ref: SAN(SCDate: Add to Reading List Source URL: www.hfs.scot.nhs.uk Language: English National Health Service NHS Scotland Adverse event NHS National Services Scotland Medical device Occupational safety and health Patient safety organization Patient safety Medicine Health Medical equipment
85	UNIVERSITY OF CALIFORNIA, SAN FRANCISCO — HUMAN RESEARCH PROTECTION PROGRAM/CHR This is only a template - other versions can be used to meet your departmental or Sponsor requirements. Adverse Event Summary Log for S Add to Reading List Source URL: www.research.ucsf.edu Language: English - Date: 2013-06-06 15:28:05 Clinical research Pharmaceutical industry Adverse event
86	Microsoft Word - Public_IRB_Member.doc Add to Reading List Source URL: www.firstclinical.com Language: English - Date: 2014-09-14 03:12:35 Science Medical ethics Pharmacology Design of experiments Bioethics Institutional review board Sham surgery Clinical trial Adverse event Clinical research Medicine Research
87	QuarterWatch Monitoring FDA MedWatch Reports Anticoagulants the Leading Reported Drug Risk in 2011 May 31, 2012 New Data from 2011 Quarters 3 - 4 Add to Reading List Source URL: www.ismp.org Language: English - Date: 2012-05-30 15:35:22 Organic chemistry Piperazines Food and Drug Administration Medical terms Pharmacy Adverse Event Reporting System Adverse effect Varenicline Levofloxacin Chemistry Medicine Pharmacology
88	THE UNIVERSITY OF NORTH CAROLINA AT CHAPEL HILL STANDARD OPERATING PROCEDURES FOR INDIVIDUAL CONFLICTS OF INTEREST AND COMMITMENT Revised August 24, 2012 I. II. Add to Reading List Source URL: www.unc.edu Language: English - Date: 2012-08-24 20:21:47 COI Adverse event Clinical research Conflict of interest Political corruption
89	Office of Human Research Ethics Daniel Nelson, Director T Add to Reading List Source URL: research.unc.edu Language: English - Date: 2012-11-27 10:01:04 Science Institutional review board Public Responsibility in Medicine and Research National Institutes of Health Adverse event North Carolina Research Campus Human subject research Grant Certified IRB Professional Clinical research Research Medicine
90	3.2 ADVERSE EVENT (AE) PROCESS & FORMS Serious Adverse Events (SAEs), Suspected Unexpected Serious Adverse Reactions (SUSARs), annual trial safety updates and other related safety information are Add to Reading List Source URL: www.sjog.org.au Language: English - Date: 2014-10-30 00:26:29 Pharmacology Science Health Design of experiments Patient safety Clinical trial Adverse effect Institutional review board Serious adverse event Clinical research Research Pharmaceutical industry

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