Pharma and Device Content We Translate
✔ Drug labeling and package inserts
✔ Patient information leaflets
✔ Instructions for use (IFUs) and user manuals
✔ Regulatory submission documents
✔ Clinical study documentation
✔ SOPs and quality documentation
✔ Device software interfaces and displays
✔ Product packaging and cartons
IFU and Labeling Translation to Regulatory Standards
Labeling is where regulation and language meet. We translate IFUs, inserts, and packaging using established regulatory phrasing in the target language, preserve symbols, warnings, and layout requirements, and deliver print-ready files through DTP—including Arabic right-to-left labeling built correctly, not mirrored as an afterthought.
Controlled Terminology, Verified Units
Active ingredients, dosage forms, storage conditions, contraindications: each has one correct rendering, and we enforce it with locked glossaries. Every value and unit is verified against the source at translation, and re-verified at editing when you order it, because a decimal slip on a label is a recall risk.
Why pharma and device teams choose Locstars
✔ Life-science specialist translators — pharma and device content only in expert hands.
✔ Regulatory-convention fluency — phrasing and formats authorities recognize.
✔ Optional double review — separate editing and proofreading available on any deliverable.
✔ Confidential by default — dossiers and product data strictly protected.
Preparing labeling or a submission?
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Handled confidentially from the first file.
