Difference between revisions of "Protecting Human Research Subjects"

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== United States Standards ==
== United States Standards ==
In the United States of America, the '''Federal Policy for the Protection of Human Subjects''' or the [https://www.hhs.gov/ohrp/regulations-and-policy/regulations/common-rule/index.html Common Rule] outlines the basic provisions for [[IRB Approval|Institutional Review Boards (IRBs)]], [[Informed Consent|informed consent]], and other aspects related to protecting the rights of '''human research subjects'''. If an institution seeks guidance on implementation of the '''Common Rule''' and other applicable federal regulations, the institution should contact the department/agency conducting or supporting the research involving human research subjects..
In the United States of America, the '''Federal Policy for the Protection of Human Subjects''', or the [https://www.hhs.gov/ohrp/regulations-and-policy/regulations/common-rule/index.html Common Rule] outlines the basic provisions for [[IRB Approval|Institutional Review Boards (IRBs)]], [[Informed Consent|informed consent]], and other aspects related to protecting the rights of '''human research subjects'''. If an institution seeks guidance on implementation of the '''Common Rule''' and other applicable federal regulations, the institution should contact the department/agency conducting or supporting the research involving human research subjects..


== European Standards ==
== European Standards ==

Revision as of 14:49, 13 January 2021

Research involving human subjects can pose complex ethical issues that require careful thought and consideration on the part of both researchers and participants. Research teams must seek ethics certifications for human subjects approval to apply for and obtain IRB approval and to protect the rights and welfare of study participants in a research project. This page will discuss the when, how, and who of ethics certifications for human research subjects.

Read First

Overview

As a prerequisite for IRB approval, all members of the research team who manage personally identifiable information (PII) must obtain ethics certifications to conduct research with human subjects. This may include principal investigators, research assistants, field coordinators, and/or survey firm staff. Two commonly accepted sources of certification are:

These courses cover the historical development of human subject protections, discuss the ethical issues involved in this human subjects research, and present the principles and regulations governing it. They are divided in modules that provide reading materials and entail quizzes for which a minimum score is required to pass each module. Learners may complete the modules at their own pace.

Certificates usually have expirations and must be renewed. The CITI certificate must be renewed every 3 years, whereas the expiration of the NIH depends. Note that the IRBs can also define a date past which the certificates are considered invalid.

United States Standards

In the United States of America, the Federal Policy for the Protection of Human Subjects, or the Common Rule outlines the basic provisions for Institutional Review Boards (IRBs), informed consent, and other aspects related to protecting the rights of human research subjects. If an institution seeks guidance on implementation of the Common Rule and other applicable federal regulations, the institution should contact the department/agency conducting or supporting the research involving human research subjects..

European Standards

(GDPR)

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