Explain your strategy to develop or obtain any IRB-required documentation. 1 ref.

Explain your strategy to develop or obtain any IRB-required documentation. 1 ref.

Subject(s): Business–Business – Other

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1. Write a 250 word response to the following:

Explain your strategy to develop or obtain any IRB-required documentation. 1 ref.

2. Reply to classmate’s post, 150 words, 1 ref.

There are several required documentation needed for any new IRB study, first the study must be approved after its acceptance by both chair members and submission to TK20. A researcher must reassure that their study was accepted by verifying email or letter. Second a researcher must prepare an informed consent document in addition to the strategy to gather consent. This consent form has most of the things IRB is looking for, from exclusion/population criteria risks etc. The informed consent form is similar to the IRB submission process. There are many other considerations when developing a new study that are part of the project submission process. Whats best is to keep it clear and concise and try to satisfy as much of the requirements as possible to remain exempt. The guidance documents or viewing the trees or the checklist in this example will help you narrow down what is a category 2 study under IRB and what isn’t. A researcher to avoid acceptance with changes must reconsider not collecting demographics as one example age zip code and certain other things that decrease anonymity for review. A combination and minimization of these categories that involve participant data ensure a category 2 as exempt under IRB. Its one of two requirements either data must be fully transparent, or the data collector or survey must ensure anonymity. A researcher must consider what they collect its a combination of the lack of demographic data, a one of two considerations of anonymity either in the method of collecting data and the data itself via identifiers.

It is useful to see the guidance documents to reassure your study poses less than minimal risks to participants based on all these specific considerations from the researcher. Another thing to consider is what information is collected from participants that any discomfort should not be greater than discomfort they experience in daily life, their workplace or working from home with my personal study highlighting stress in their life. How such topics would lead local Institutional Review Boards (IRB) to exercise more oversight than when topics were not so sensitive (Loseke, 2017). From question and method used and its inherent strategies these aspects are essential for IRB to deem a study as exempt or approved. In my case consent is a required (e.g. click to submit/continue) checkbox as the landing page on a crowdsourcing system. I will not collect name or email for informed consent. The next step for IRB is to have in hand a copy of the questionnaires associated with the study in which in my case are part of an interview rather internet survey hybrid format (e.g. open ended questions internet survey). Additional documentation for the IRB are any site permissions, any communication with a previous company in this example pharmaceutical companies that were interested or OK the study during its development, instrument permissions as some instruments require permission from the researcher and its modification, permission to use data, and any other document that approves the study from the University of Phoenix as well as previous reviews from IRB between its approval and decisions with either approved with conditions, information required or modifications required.