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An institutional review board (IRB), also known as an independent ethics committee (IEC), ethical review board (ERB), or research ethics board (REB), is a committee at an institution that applies research ethics by reviewing the methods proposed for research involving human subjects, to ensure that the projects are ethical.
When registering an IRB, the following information must be provided to OHRP: the information of the institution, including its name and mailing address, the personal information of the person in charge of the IRB, the estimated number of active protocols that the IRB has conducted an initial review or is going to conduct a review, and the ...
This is known as the internal ratings-based (IRB) approach to capital requirements for credit risk. Only banks meeting certain minimum conditions, disclosure requirements and approval from their national supervisor are allowed to use this approach in estimating capital for various exposures.
It was based on the Nuremberg Code, focusing on medical research with therapeutic intent. Subsequently, medical professionals and researchers began requiring that research follows the principles outlined in the Declaration. This document was one of the milestones towards the implementation of the institutional review board (IRB) process. [9]
IRB 101 sm (an introduction to the history and regulations that govern the institutional review board (IRB)), [19] IACUC 101 (an overview of the laws, regulations, and policies that govern the humane care and use of laboratory animals), IRB 201 (a detailed look at the criteria for review of research protocols),
Detailed protocols for proposed clinical studies to assess whether the initial-phase trials will expose the subjects to unnecessary risks. Other commitments are commitments to obtain informed consent from the research subjects, to obtain a review of the study by an institutional review board (IRB), and to adhere to the investigational new drug ...
The site is usually a hospital or a similar health care institution that has adequate infrastructure and staff to meet the requirements of the clinical trial protocol. The scope of an SMO's responsibility is limited to the site and hence the eponymous title. Some (but not all) of the responsibilities include: Contract
This page is an attempt to establish such a research protocol. It takes the form of a pledge or agreement between the ethnographer and the Wikipedian community. It is not the only possible research protocol, but it can be used by any researcher who wishes to ethically research Wikipedia by actively interacting with the community.