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IRB: Ethics
Results: 397

#	Item
201	IRB Children supp. Version 2 Add to Reading List Source URL: archive.hhs.gov Language: English - Date: 2005-08-30 07:32:18 Medical ethics Design of experiments Pharmacology Research ethics Institutional review board Human subject research Consent Ethical problems using children in clinical trials Informed consent Ethics Clinical research Research
202	Columbia University IRB New page: Informed Consent (required for all studies) Select all that apply: Add to Reading List Source URL: www.cumc.columbia.edu Language: English - Date: 2013-08-20 10:22:36 Medical ethics Behavior Informed consent Consent Research Ethics Autonomy Clinical research
203	Building 2 Greenstone Hill Office Park Emerald Boulevard Modderfontein PO Box 8237 Greenstone 1616 Johannesburg South Africa Tel[removed]Fax[removed]E-mail [removed] Docex DX008 Edenvale Internet www.irb Add to Reading List Source URL: www.ifac.org Language: English - Date: 2014-08-18 08:21:30 External auditor Internal audit Audit International Ethics Standards Board for Accountants Accountant Auditor independence Statement on Auditing Standards No. 70: Service Organizations Auditing Accountancy Business
204	Microsoft Word - American University IRB Application Checklist Add to Reading List Source URL: www.american.edu Language: English - Date: 2014-06-30 14:38:20 Pharmaceutical industry Public Responsibility in Medicine and Research Consent Deception Experimentation on prisoners Institutional review board Clinical research coordinator Ethics Clinical research Behavior
205	Columbia University IRB New page: Informed Consent (required for all studies) Select all that apply: Add to Reading List Source URL: cumc.columbia.edu Language: English - Date: 2013-08-20 10:22:59 Medical ethics Behavior Informed consent Consent Research Ethics Autonomy Clinical research
206	Columbia University IRB Guidance for Collaborating Individual Investigators October 29, 2013 This document provides guidance relating to the use of Individual Investigator Agreements to extend the coverage of Columbia Un Add to Reading List Source URL: www.cumc.columbia.edu Language: English - Date: 2013-10-29 16:29:21 Research Drug safety Scientific method Ethics Institutional review board Institute of Internal Auditors Clinical research coordinator Cooperative Human Tissue Network Clinical research Design of experiments Pharmacology
207	RESEARCH SUBJECTS INFORMATION UPDATED CUMC INSTITUTIONAL REVIEW BOARD (IRB) CONTACT INFORMATION The Columbia University Medical Center (CUMC) Institutional Review Board (IRB) is a committee that independently conducts on Add to Reading List Source URL: www.cumc.columbia.edu Language: English - Date: 2013-10-16 13:31:46 Medical ethics Applied ethics Design of experiments Pharmacology Drug safety Institutional review board Informed consent Human subject research Clinical research coordinator Clinical research Research Ethics
208	Columbia University IRB Policy Data Security Plans Involving the Use, Storage or Transmission of Electronic Research Data Constituting Sensitive Data I. Background Add to Reading List Source URL: www.cumc.columbia.edu Language: English - Date: 2013-11-18 10:30:22 Computer security Law Data security Privacy law Computer law Information security Personally identifiable information Health Insurance Portability and Accountability Act Payment Card Industry Data Security Standard Data privacy Security Ethics
209	Microsoft Word - NPS IRB Interim Guidance for Survey Research (LGS) 25 Apr 2013 Add to Reading List Source URL: www.nps.edu Language: English - Date: 2013-05-02 18:37:31 Drug safety Institutional review board Ethics Scientific method Science Cooperative Human Tissue Network Clinical research Design of experiments Pharmacology
210	The CUMC IRB is pleased to announce our Spring Schedule for Educational Sessions: Monthly Investigator Meetings: These sessions will be held once a month to help ensure that all human subjects research is conducted in a Add to Reading List Source URL: cumc.columbia.edu Language: English - Date: 2013-01-08 12:20:53 Pharmacology Science Institutional review board Ethics WebAPI Sundial Measurement Review Board Clinical research Drug safety Design of experiments

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