Products
Numbers, doses and units are checked against the source document automatically; segments that do not match are flagged for review. The dictation transcript is kept unchanged, and the report draft stays linked to it.
The terminology glossary, user roles, facility scope and quotas are set by the institution's own administrator. Accounts are invitation-only, and every request is authorized server-side by institution, facility, product and action.
Memoris acts only as a data processor and handles clinical content solely on the institution's instructions. Documents are stored in the EU (Germany). Content reaches language and speech providers only at processing time, under no-logging and no-training terms.