We would like to thank everyone, who attended our webinar on changes in EBA 2.10 reporting framework. More changes are coming and at BR-AG we are monitoring these closely so follow us on LinkedIn:
Also, feel free to reach out for more information.
Following up on the Q&A session during our webinar, we collected questions passed on by attendees and would like to share them with as well.
What we know from experience, that except of supporting a given regulatory frameworks e.g. EBA CRD IV / CRR the reporting tool should run data validation checks against both XBRL and non-XBRL rules (when taxonomy issuer (EBA/EIOPA) introduces new version of taxonomy not all validation rules are reflected in the published list of business validations). Apart from that it is appreciated when the tool has a comprehensive validation errors display panel in which you could find all the necessary information – tables and cells affected by the error, exact validation code from the taxonomy and mathematical logic of the error. Lastly, most errors are human errors, so the regulatory reporting software should be as intuitive and user-friendly as possible.
That is correct, we expect that DPM v2.10 phase 2 will contain Covid-19 measures reports, at the moment we assume that EBA will publish the package on 10th of July, but slight delays are possible. Regarding the implementation in ATOME: Particles, it will take probably a week from the moment of publication by the EBA.
If there are any other questions that you would like to discuss or you would like to have a closer look at the technology that was used to present the EBA framework, please feel free to contact us – we will be happy to help.
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