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This is a question from a department of Health policy staff member. She has noted that there is a general lack of data on equity and it is of interest to many different parties. Do any of you formally require/recommend that researchers include data on equity in their research?
I have been considering requiring an annual status report in leu of Continuing Review where this information would be captured, including, if informed consent required, the breakdown of Spanish-speaking consent used vs. English-speaking.