The goal of this study was to describe the contributions of community members (unaffiliated members) who serve on institutional review boards (IRBs) at large medical research centers and to compare their contributions to those of other IRB members. We observed and audiotaped 17 panel meetings attended by community members and interviewed 15 community members, as well as 152 other members and staff. The authors coded transcripts of the panel meetings and reviewed the interviews of the community members. Community members played a lesser role as designated reviewers than other members. They were infrequently primary reviewers and expressed hesitation about the role. As secondary or tertiary reviewers, they were less active participants than o...
PURPOSE: To determine how closely institutional review board (IRB) discussions reflect the ethical c...
Background: Although variations among institutional review boards (IRBs) have been documented for 30...
Ethical research involving human subjects mandates that individual informed consent be obtained from...
The practice of maintaining large Institutional Review Boards (IRBs) raises the question whether mem...
Purpose: The roles of nonaffiliated and nonscientific institutional review board (IRB) members at ac...
Oversight of human subject research has evolved considerably since its inception. However, previous ...
all medical research so as to appreciate the broad context of IRB work. Methods We have collected da...
In the U.S., all research must be approved by an Institutional Review Board (IRB) that evaluates res...
With the growing trend of community-based research, academic-based Institutional Review Boards (IRBs...
Background: We report on the challenges of obtaining Institutional Review Board (IRB) coverage for a...
Institutional review boards (IRBs) are instruments of social control that provide a formal regulator...
Institutional Review Boards (IRBs)—committees responsible for the protection of human subjects in me...
poster abstractCommunity members (i.e., community advisory boards or CABs) give researchers priceles...
This study explored the effects of integrating community members into the evaluation of clinical and...
ABSTRACT National and international codes of research conduct have been established in most industri...
PURPOSE: To determine how closely institutional review board (IRB) discussions reflect the ethical c...
Background: Although variations among institutional review boards (IRBs) have been documented for 30...
Ethical research involving human subjects mandates that individual informed consent be obtained from...
The practice of maintaining large Institutional Review Boards (IRBs) raises the question whether mem...
Purpose: The roles of nonaffiliated and nonscientific institutional review board (IRB) members at ac...
Oversight of human subject research has evolved considerably since its inception. However, previous ...
all medical research so as to appreciate the broad context of IRB work. Methods We have collected da...
In the U.S., all research must be approved by an Institutional Review Board (IRB) that evaluates res...
With the growing trend of community-based research, academic-based Institutional Review Boards (IRBs...
Background: We report on the challenges of obtaining Institutional Review Board (IRB) coverage for a...
Institutional review boards (IRBs) are instruments of social control that provide a formal regulator...
Institutional Review Boards (IRBs)—committees responsible for the protection of human subjects in me...
poster abstractCommunity members (i.e., community advisory boards or CABs) give researchers priceles...
This study explored the effects of integrating community members into the evaluation of clinical and...
ABSTRACT National and international codes of research conduct have been established in most industri...
PURPOSE: To determine how closely institutional review board (IRB) discussions reflect the ethical c...
Background: Although variations among institutional review boards (IRBs) have been documented for 30...
Ethical research involving human subjects mandates that individual informed consent be obtained from...