Does a lower-risk workflow mean lower accuracy for regulatory submissions?

No. The accuracy requirement does not change for administrative documents, supporting correspondence, routine updates or lower-complexity annexes. Translated regulatory submissions must always accurately and completely reflect the approved source. A lower-risk workflow may be appropriate when the document type, product context, submission purpose, target authority, target markets and client-side controls support that choice. Different workflows manage the probability and consequences of translation error, not the accuracy objective itself. For clinical evidence, safety information, product information and authority-facing technical content, stronger workflows are usually more appropriate.