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Informed consent
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251	Stanford University HRPP Informed Consent Checklist Medical Research, Clinical Investigations CHK-C1m 1/4 Add to Reading List Source URL: humansubjects.stanford.edu Language: English - Date: 2014-06-26 16:17:02 Medical research Clinical research Clinical research ethics Pharmaceutical industry Medical ethics Design of experiments Clinical trial Title 1 of the Code of Federal Regulations Health Insurance Portability and Accountability Act Informed consent
252	Informed consent information should be consistent with procedures, etc. as described in eProtocol application VA research: Refer to CHK-7 VA Research and AID-27m Reviewing VA Research for additional requirements Regul Add to Reading List Source URL: humansubjects.stanford.edu Language: English - Date: 2014-08-06 19:30:22 Medical research Clinical research Clinical research ethics Pharmaceutical industry Medical ethics Design of experiments Title 1 of the Code of Federal Regulations Clinical trial Health Insurance Portability and Accountability Act Informed consent
253	CTO Clinical Trial Informed Consent Form Template Instructions: This Clinical Trial Informed Consent Form (ICF) Template has been designed to meet current regulatory and ethical standards. The study-wide (provincial) Add to Reading List Source URL: www.ctontario.ca Language: English - Date: 2015-10-07 13:14:50
254	THE UNIVERSITY OF HONG KONG Human Research Ethics Committee Add to Reading List Source URL: www.rss.hku.hk Language: English - Date: 2016-01-04 23:10:32 Medical ethics Clinical research ethics Human subject research Autonomy Clinical research Informed consent Institutional review board Consent Medical privacy Research Internet Psychology
255	Best Practices for Gathering Informed Consent & the Content of Consent Forms October 1, 2015 – Alyx Larocque, Analyst Express consent is informed and voluntary. Consent is informed when the individual knows the purpose Add to Reading List Source URL: www.oipc.sk.ca Language: English - Date: 2015-10-02 14:55:42
256	Protocol Director: Protocol: Name of Test Article: include IND/IDE Number, if applicable Add to Reading List Source URL: humansubjects.stanford.edu Language: English - Date: 2012-02-06 15:25:51 Medical ethics Medical research Clinical research ethics Applied ethics Ethics Human subject research Informed consent Consent
257	Minimum Criteria for ICH E6 GCP Investigator Site Personnel Training (Excerpt from TransCelerate BioPharma Operating Principles) Scope The intent of this document is to define the Minimum Criteria for Good Clinical Pract Add to Reading List Source URL: www.transceleratebiopharmainc.com Language: English - Date: 2015-12-07 16:54:46 Medical research Clinical research Pharmaceutical industry Good clinical practice Adverse event Source document Public Responsibility in Medicine and Research Informed consent Inclusion and exclusion criteria Serious adverse event Human subject research Trial master file
258	Informed Consent [FOCUS GROUP RESEARCH] Study Title You are invited to participate in a research study about [PURPOSE OF STUDY]. This study is being conducted by [NAME AND AFFILIATION OF RESEARCHERS]. [FUNDING SOURCE] Add to Reading List Source URL: or.nd.edu Language: English - Date: 2014-10-23 14:34:29
259	VCC Choice and Consent Working Group, draft: 6-Sep-13 _____________________________________________________________________________________________ CHOICE AND CONSENT – Policy principles related to the customer’ Add to Reading List Source URL: www.smartgrid.gov Language: English - Date: 2015-02-12 06:56:56 Medical ethics Autonomy Ethics Identity management Applied ethics Law Human subject research Informed consent Privacy Internet privacy Consent
260	USC HSIRB Informed Consent Template and Instructions June 2014 General Instructions for Using the Template Add to Reading List Source URL: oprs.usc.edu Language: English - Date: 2014-06-06 13:54:44

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