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LIFE SCIENCES
Content where terminology and context are critical
We support medical and pharmaceutical projects that require controlled terminology, reference-document consistency and multi-step linguistic QA.
01Clinical TrialsProtocols, ICF/PIS, Investigator’s Brochures, CRFs, CSRs, study correspondence and site materials.
02PharmacovigilanceSafety content, PV procedures, safety narratives and documentation related to adverse-event reporting.
03Medical DevicesIFUs, labeling, interface content, technical documentation and user-facing device materials.
04Pharma & RegulatoryProduct information, regulatory documentation, quality documentation, and specialist communications.
05Healthcare & Patient MaterialsMedical records, patient-facing materials, and communications for healthcare professionals.
06Revision & QABilingual revision, proofreading, backtranslation review, terminology control and final linguistic QA.
QUALITY WORKFLOW
Terminology control from first segment to delivery
We adapt to client TMs, glossaries, style guides, reference documents, and reviewer workflows. We can deliver changes in tracked-changes format or directly in bilingual production files.
Client glossary & terminology rules
CAT / bilingual files / TM
Reviewer & tracked-changes workflows
Reference-document consistency
Tags, numbers & formatting QA
Final linguistic QA
PROJECT EXPERIENCE
Pharma and healthcare in practice
Our linguists have worked on medical and pharmaceutical projects, including assignments delivered through translation-agency partners.
BayerPolpharmaHerbapolClinical ResearchMedical DevicesPharmacovigilance
LANGUAGES
Polish and English at the core of our specialization
PL ↔ UAEN ↔ UAUA ↔ other foreign languages
