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.
- Provide the Brief Summary, Purpose and the Research Questions from the study in your own words. It is not required for you to provide the Data Collection Tools, Data Points Yielded or the Data Source but the Data Analysis should be summarized for the study. A sample of what is asked regarding proposed procedures can be found at #11 on the Walden IRB Application from the sample IRB Application linked above.
- Provide a descriptive and evaluative summary of the study with particular focus on the results and discussion sections.
- Cite the medical study chosen to use as the basis for completing a sample IRB Application form.
- The document should be 1-2 pages, written in APA style.
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In A World Cup Soccer Match Juan Is Running Due North Toward The Goal With A Spe 1
/in Uncategorized /by developerIn a World Cup soccer match, Juan is running due north toward the goal with a speed of 7.60 { m/s} relative to the ground. A teammate passes the ball to him. The ball has a speed of 13.0 { m/s} and is moving in a direction of 36.9 DEGREE east of north, relative to the ground.What is the magnitude of the ball’s velocity relative to Juan?What is the direction of the ball’s velocity relative to Juan?
Juan speed is 7.6 m/s towards northBall speed is 13.0 m/s towards 36.9o east of north By resolving components of ball’s velocity,In north, vn = 13.0 cos(36.9o) = 10.4 m/sIn east, ve = 13.0 sin…
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In A World Cup Soccer Match Juan Is Running Due North Toward The Goal With A Spe
/in Uncategorized /by developerIn a World Cup soccer match, Juan is running due north toward the goal with a speed of 7.20 m/s relative to the ground. A teammate passes the ball to him. The ball has a speed of 12.1 m/s and is moving in a direction of 33.4 degrees east of north, relative to the ground.What is the magnitude of the ball’s velocity relative to Juan?Answer in m/sWhat is the direction of the ball’s velocity relative to Juan?Answer in degrees north of east.
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In A World Of Corporate Taxes Only Show That The Wacc Can Be Written As Wacc Ru
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Question:In a world of corporate taxes only, show that the WACC can be written as WACC = RU * [1 Tc(D/V)].Solution:WACC = RU * [1 – Tc(D/V)]Where asRu = cost of DebtTc = Tax rateD/V = Debt…
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In A Young S Double Slit Experiment The Separation Between The Slits Is 1 20 104
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In A Young S Double Slit Experiment Two Rays Of Monochromatic Light Emerge From
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In About 100 Words State The Importance Of Reliable Information And Clinical Dat
/in Uncategorized /by developerIn about 100 words state the importance of reliable information and clinical data for providing high-quality patient care. You are welcome to research this topic over the web and provide examples to substantiate your answer.
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In About 5 Billion Years At The End Of Its Lifetime Our Sun Will End Up As A Whi
/in Uncategorized /by developerIn about 5 billion years, at the end of its lifetime, our sun will end up as a white dwarf, having about the same mass as it does now, but reduced to about 15,000 km in diameter.What will be its density at that stage?
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In Acc 522 The Discussion Question Is A Corporation Has Identified A Target Comp
/in Uncategorized /by developerIN ACC 522 the discussion question is: A corporation has identified a target company to acquire. It is trying to decided on the best strategy, that is whether to acquire the target with a stock issuance or with cash. Assume the acquiring company can do either, what are the tax advantages and disadvantages of using cash versus credit for the acquisition? What would your advice be in this situation? Why?
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In Access Use The School Table To Make A Query That Lists The Schools That Are E
/in Uncategorized /by developerin ACCESS, Use the School table to make a query that lists the schools that are either located in an urban area with a population of at least 250,000 (ULOCAL=11) or are charter schools (CHARTR=1). Show the school name, phone, city, ULOCAL and CHARTR. Order the results by City. Name the query “Large or Charter” (without the quotes). [11 points]
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In Accordance With The U S Food And Drug Administration An Institutional Review
/in Uncategorized /by developerIn 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.
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