In some cases, the data entered into GloBE-Reg will be assessed for quality on an annual basis. This exercise will only occur when an active GloBE-Reg study has specified the requirement for regular quality assurance (QA) in the Research Request Form and has considered the additional costs that are associated with this. For each participating centre, a maximum of 10% of the cases (or a minimum of 1) that are included in the study for each clinician responsible shall be eligible for a remote QA. For these eligible cases, the centre will be invited to submit evidence through the QA platform integrated within the Registry. The GloBE-Reg team will arrange to meet the Centre and discuss the process in more detail and provide further guidance.
Last Modified