Discuss role of the irb in reviewing and approving protocols


Assignment task:

We have discussed the Role of the IRB in reviewing and approving protocols and consent forms in class.  We have also discussed ethical considerations and issues with genetic research.

Your writing assignment is to consider yourself as a member of the Breakthrough University Institutional Review Board.  Breakthrough University is located in the United States and FDA and Department of Health and Human Services regulations are applicable.  One of the physician researches, Professor Dr. Alvin Funk, has submitted a protocol for a Phase II Gene Transfer study to evaluate his new gene therapy in patients with refractory, late-stage ovarian cancer.  The Chairman of the IRB has asked you to take a lead on reviewing the informed consent form.  You need to inform the entire IRB Board at the next meeting what are the three most important aspects to consider in reviewing the consent form language.  In other words, what are the three most important things you need to look for in the draft consent form-and if they are not in the consent form, you would recommend the inclusion of these items.

This writing assignment should not exceed two standard pages (single spaced) or four standard pages (double spaced) in no less than 12-point font.  Title and reference pages are not included in the page limit.  Concisely discuss your three most important items for the consent and your reasons for choosing them including any basis in the regulations, ethical considerations and support for your position from the Belmont Report. Please also provide me with the reference

Request for Solution File

Ask an Expert for Answer!!
Other Subject: Discuss role of the irb in reviewing and approving protocols
Reference No:- TGS03350316

Expected delivery within 24 Hours