When the content is clinical, precision isn't a preference, it's a requirement.
In your healthcare content a mistranslation isn't an inconvenience, it's a patient-safety and regulatory risk. We run the operation that keeps your clinical and regulatory content exact, terminology controlled, and accountable across every market you supply.
The commercial question underneath it: EU medical device rules oblige instructions and labelling in the official language of every member state you supply, which can mean up to 24 languages, regenerating with every product revision.
Where healthcare content breaks.
Regulatory accuracy, patient safety, and terminology that leaves no room for ambiguity in any market.
In healthcare content, ambiguity is a safety risk. We enforce validated terminology and maintain the audit trail your regulated markets require.
One programme, tuned to your sector.
The problem is never only linguistic. It is structural: the brief loses context at handoff, terminology drifts across markets and content types, and no single party is accountable for whether the output lands. That is an operations problem, and it has an operations solution.
Brief discipline. Every piece of healthcare content starts with a structured brief captured at intake, not lost in an email thread.
Terminology enforcement. One termbase, maintained by us, applied across your regulatory submissions, clinical documentation, patient material, and medical device content, consistent in every market.
Risk-tiered routing. Your high-volume content moves on machine throughput with automated checks. Anything with brand, legal, or compliance exposure routes to human judgment.
The same operating model, across fourteen industries.
What is your healthcare content costing you per market?
The audit quantifies it, built on public data, delivered board-ready.
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