This document summarizes the topics that need to be addressed in a proposal for human research -- confidentiality, protection of participants from harm, consent, etc. This document was developed in the late 1990\u27s and the consent form guidelines have gone through much revision at Simon\u27s Rock (and, of course, all studies will have their own specific ethical and human subject issues to address), but this provides a good starting point or initial guide
Activities such as continuous quality improvement, comparative effectiveness research, and electroni...
1. Review ongoing changes in expectations about data availability affecting scholarly communication ...
An introduction to Human Subjects Research: Understanding the regulatory background, IRB submission...
Most individuals outside of research are unaware of the function of an Institutional Review Board (I...
Institutional review boards (IRBs) protect the health, safety, and privacy of people participating i...
The IRB is a body of professional and lay persons who review all research studies from an institutio...
The first question a researcher should consider with respect to IRB review is whether the research p...
Ethics has gained much popularity and recognition in the field of research with the development of b...
This guidance document assists UCLA investigators with determining which activities require UCLA OHR...
The Institutional Review Board (IRB), also known as an Independent Ethics Committee (IEC), is the mo...
To describe policies and procedures for determining the types of activities that qualify as human re...
This document aims to propose guidelines for human rights considerations, similar to the work done o...
The history of health research, and concerns about the protection of human participants, dates back ...
Institutional review boards (IRBs) are responsible for regulating and safeguarding research with hum...
After Reading This Chapter, You Will: Have a general knowledge of Institutional Review Board (IRB) p...
Activities such as continuous quality improvement, comparative effectiveness research, and electroni...
1. Review ongoing changes in expectations about data availability affecting scholarly communication ...
An introduction to Human Subjects Research: Understanding the regulatory background, IRB submission...
Most individuals outside of research are unaware of the function of an Institutional Review Board (I...
Institutional review boards (IRBs) protect the health, safety, and privacy of people participating i...
The IRB is a body of professional and lay persons who review all research studies from an institutio...
The first question a researcher should consider with respect to IRB review is whether the research p...
Ethics has gained much popularity and recognition in the field of research with the development of b...
This guidance document assists UCLA investigators with determining which activities require UCLA OHR...
The Institutional Review Board (IRB), also known as an Independent Ethics Committee (IEC), is the mo...
To describe policies and procedures for determining the types of activities that qualify as human re...
This document aims to propose guidelines for human rights considerations, similar to the work done o...
The history of health research, and concerns about the protection of human participants, dates back ...
Institutional review boards (IRBs) are responsible for regulating and safeguarding research with hum...
After Reading This Chapter, You Will: Have a general knowledge of Institutional Review Board (IRB) p...
Activities such as continuous quality improvement, comparative effectiveness research, and electroni...
1. Review ongoing changes in expectations about data availability affecting scholarly communication ...
An introduction to Human Subjects Research: Understanding the regulatory background, IRB submission...