Aspect Translations

Aspect helps CROs, pharmacovigilance vendors, eCOA providers, pharmaceutical companies and biotech teams manage multilingual regulated content without losing control of terminology, document versions or timelines. We support: Clinical trials — protocols and amendments, investigator brochures, informed consent forms, patient-facing materials, site documents and regulatory correspondence Pharmacovigilance and drug safety — ICSR narratives and source documents, DHPCs, PSUR/PBRERs, RMPs and risk-minimization materials eCOA and digital patient solutions — platform strings, PRO instruments, forward and back translation, reconciliation and in-context linguistic QA Regulatory and labeling — SmPCs, PILs, labels, IFUs, submissions and regulatory correspondence Our workflow combines qualified medical linguists, translation–editing–proofreading, independent quality control, dedicated clinical project management, terminology management, translation memory and amendment tracking. Aspect has more than 15 years of experience and supports 30+ languages across Central and Eastern Europe, the Baltics, Balkans, Caucasus and additional markets. Our quality management system is certified to ISO 9001, and our information-security management system is certified to ISO 27001. Projects are handled through secure workflows supported by dedicated private servers hosted in Germany. We help clients reduce linguistic and regulatory risk, keep multilingual documents aligned through amendment cycles, meet time-critical deadlines and deliver audit-ready files. Project enquiries: project@aspect-translations.com