IRB: Ethics

Results: 397



#Item
41Medical ethics / Clinical research ethics / Human subject research / Design of experiments / Institutional review board / Consent / Informed consent

REQUEST FOR CHANGE IN CAMPUS IRB APPROVAL UNIVERSITY of MISSOURI - ROLLA (UMRIRB-2) Review Requested: Amendment ____ Revision ____ Addendum ____ Other ____ *This form is not intended to be used for continuing rev

Add to Reading List

Source URL: irb.mst.edu

Language: English - Date: 2014-01-22 05:22:59
42Medical ethics / Clinical research ethics / Clinical research / Design of experiments / Research ethics / Institutional review board / Public Responsibility in Medicine and Research / Human subject research / Food and Drug Administration / IRB / Clinical research coordinator / Clinical trial

Microsoft Word - SOP - Board Purpose and Function.doc

Add to Reading List

Source URL: research.missouri.edu

Language: English - Date: 2015-07-01 12:40:12
43Grant / Philanthropy / Clinical research ethics / Pharmaceutical industry / Design of experiments / Clinical research / Institutional review board / Cooperative Human Tissue Network

Information about the required Human Subjects narrative For the IRB Human Subjects narrative, you will need information from the “Documents and Instructions” section of the electronic application “IRB Information f

Add to Reading List

Source URL: fellowships.international.wisc.edu

Language: English - Date: 2016-03-21 12:35:31
44Clinical research ethics / Human subject research / Medical ethics / Design of experiments / Institutional review board / Informed consent / IRB / Clinical research coordinator / Public Responsibility in Medicine and Research

https://webirb.research.ucla.edu/WEBIRB/Doc/0/DON519E1RMF47FBIJJ4B0757BE/fromString.html  

Add to Reading List

Source URL: www.heri.ucla.edu

Language: English - Date: 2015-12-03 12:51:38
45Clinical research ethics / Medical ethics / Clinical research / Design of experiments / Human subject research / Institutional review board / Public Responsibility in Medicine and Research / Office for Human Research Protections / Certified IRB Professional / Clinical research coordinator

Stanford University HRPP International Research

Add to Reading List

Source URL: humansubjects.stanford.edu

Language: English - Date: 2016-04-12 01:21:49
46Clinical research / Medical ethics / Design of experiments / Research ethics / Public Responsibility in Medicine and Research / IRB / Expanded access / Human subject research / Institutional review board / Clinical research coordinator

Table of Contents - Stanford HRPP Policy Manual chapter 1................................................................................................................................................ 1

Add to Reading List

Source URL: humansubjects.stanford.edu

Language: English - Date: 2016-08-12 17:42:03
47Clinical research ethics / Medical ethics / Design of experiments / Clinical research / Institutional review board / Office for Human Research Protections / Common Rule / Grant / IRB / Human subject research / Cooperative Human Tissue Network / Clinical research coordinator

Title: FO 306 – Institutional Review Board Authorization Agreements for Review by External IRBs (IRB Reliance) Department: Sparrow Institutional Review Board 1.0 Policy:

Add to Reading List

Source URL: www.sparrow.org

Language: English
48Medical ethics / Clinical research / Human subject research / Design of experiments / Informed consent / Clinical trial / Consent / Research participant / Placebo-controlled study / Food and Drug Administration / Clinical research coordinator / Institutional review board

Stanford University IRB Guidance

Add to Reading List

Source URL: humansubjects.stanford.edu

Language: English - Date: 2016-04-12 01:21:51
49Clinical research ethics / Research / Contact / Office for Human Research Protections / Applied ethics

The IRB staff and the IRBs have the following written policies and procedures for determining the risks to vulnerable populations as defined in applicable federal regulations, and specifically for determining the require

Add to Reading List

Source URL: humansubjects.stanford.edu

Language: English - Date: 2016-04-12 01:21:50
50Clinical research ethics / Design of experiments / Drug safety / Institutional review board / IRB

November 3, 2015 Michael Bailey Electrical & Computer Eng ECE 442 CSL

Add to Reading List

Source URL: mdbailey.ece.illinois.edu

Language: English - Date: 2015-11-04 15:13:28
UPDATE