In accordance with the U.S. Food and Drug Administration, an institutional review board (IRB) has the authority to approve or reject a biomedical research study that involves human subjects. The

In accordance with the U.S. Food and Drug Administration, an  institutional review board (IRB) has the authority to approve or reject a  biomedical research study that involves human subjects. The IRB is set  up to protect the rights of participants in research, and to do this,  IRB members use a group process to evaluate applications for research.  In this Application, you will go through the motions of constructing a  Summary for a Protocol Approval Application to an IRB as if you are the  principal investigator for a research project that involves humans as  the research subjects. To prepare for this Application, search the Internet  and download an application form for IRB Approval of Human Subjects  Research . Explore the Internet for more information on the application  process as can be found at the following Web sites: https://www.fda.gov/ScienceResearch/SpecialTopics/RunningClinicalTrials/GuidancesInformationSheetsandNotices/ucm113709.htm For this Application: Find a published medical study published within the  last 36 months of today’s date to use as the basis for completing a  sample IRB application. A scholarly journal should be used such as the  American Medical Association Journal. Scholarly medical journals can be  found in the Walden library. Next, assume that you are the principal investigator.

Do you need us to help you on this or any other assignment?


Make an Order Now