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Comment: Moving content from Tip to step & simplifying.

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abstractsafety
abstractsafety
The information you are required to provide depends on the Board approval status and other indicators, as noted in the instructions that follow. Human subject safety information is optional for Abbreviated trials.
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6127
6127

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titleLocate the IRB approval document before you begin

You will need the IRB approval document for a single site to abstract this category of information.

The only field that you are required to complete in this section is the Board Approval Status. Other fields are either optional or non-editable. The latter are indicated by gray fields.

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