Article 81 — Implementing acts
The Commission may, by means of implementing acts, establish the detailed arrangements and procedural aspects necessary for the implementation of this Chapter as regards the following:
the functioning of the electronic system referred to in Article 73;
the exchange of information between Member States as referred to in Article 76;
harmonised electronic forms for the reporting of serious adverse events and device deficiencies as referred to in Article 80;
the timelines for the reporting of serious adverse events and device deficiencies, taking into account the severity of the event to be reported as referred to in Article 80;
uniform application of the requirements regarding the clinical evidence or data needed to demonstrate compliance with the general safety and performance requirements set out in Annex I.