how do you expect data collection to be handled for Trusts where the diagnostic process takes place at one Trust whilst the first treatment may be elsewhere?
Trusts across a Cancer Network will organise the collection of data for the audit in different ways. The data collection system will allow a user (depending on access rights) to either add to or amend a patient record that is already in the system. Therefore, it is possible for one trust to enter the patient demographics and diagnostic details and another trust to enter the treatment details.
Related Questions
- how do you expect data collection to be handled for Trusts where the diagnostic process takes place at one Trust whilst the first treatment may be elsewhere?
- Can XBRL GL add efficiency to the data collection process for sustainability (corporate citizenship) reporting?
- How long will the process of data collection take ?
