Do MDSAP audits cover European requirements?

The MDSAP program does not currently address European requirements from the EU's medical device regulations (MDR and IVDR). However, several MDSAP AO are also designated Notified Bodies under these regulations and can perform combined audits under both certification schemes. If so, these AO have the option of recording the outcome of the audit in a single combined audit report or issue separate audit reports, according to their internal policies.