From clinical trials to patient information leaflets, Skriptó delivers medically accurate, regulator-ready translations—on time and with full confidentiality.
Our translators aren’t generalists—they’re scientists, MDs, or trained medical linguists. We understand the technical depth and the regulatory demands behind your documents.
We comply with EMA, FDA, and local requirements.
You’ll never have to “clean up” a translation to meet formatting or submission standards.
We meet your deadlines, even tight ones.
When you’re up against trial timelines, we mobilize the right resources quickly.
We build and maintain translation memories for your organization.
This ensures consistency across updates, product lines, and global teams.
From clinical data to product specs, your information is protected.
We sign NDAs, encrypt files, and operate under strict data control protocols.
We only work with translators who specialize in medicine, life sciences, or regulatory affairs. Each project is handled with scientific understanding and linguistic precision.
with your medical/regulatory team
by native-speaking medical translator (with scientific background)
by second reviewer or QA expert (option: in-country medical reviewer)
Request a quote, ask a question, or receive a free sample.
“Skriptó handled all translations for our Phase III trial, patient forms, investigator brochures, safety documents. Everything was clear, compliant, and delivered fast. Our ethics committee had zero remarks. That says it all.”
“With constant changes in labelling regulations, we needed a partner we could trust. Skriptó translated all SmPCs and packaging texts with perfect terminology and formatting, ready for submission to the EMA without revision.”
“We launched our medical device across 9 markets in 3 months. Skriptó translated our IFUs and user guides with medical precision and consistency. No delays, no surprises, just peace of mind.”
Whether you need multilingual clinical trial docs or fast label updates, we’re here to help.