Certified medical and pharmacological translation by licensed clinical specialists—featuring back-translation and regulatory compliance for FDA, EMA, and international trials.
In life sciences, medical translation is not just an administrative task—it is a patient safety imperative. A misplaced decimal, an ambiguous drug interaction term, or an imprecise contraindication note can halt clinical trials, trigger regulatory rejections, or compromise patient health.
IJRDO delivers an audit-ready medical localization ecosystem. All translations are performed exclusively by native physicians, pharmacologists, and certified medical linguists following ISO 17100 and ISO 13485 standards. We safeguard your clinical validity at every stage.
Protocols, Investigator’s Brochures (IB), Case Report Forms (CRF), Subject Diaries, and SAE reports.
Informed Consent Forms (ICF), Patient Reported Outcomes (ePRO), recruitment flyers, and questionnaires.
Common Technical Documents (CTD), Summaries of Product Characteristics (SmPC), and Package Leaflets (PL).
Operator manuals, software GUI strings, hazard warnings, IFUs, and compliance declarations.
Required by Institutional Review Boards (IRBs) and health authorities globally. We perform forward translation, independent blind back-translation into the source language by a separate linguist, and comparative reconciliation with a detailed discrepancy report.
Need a formal NDA executed prior to submitting your trial documents? We provide signed bilateral NDAs within 1 business hour.
Request Mutual NDA & Consultation →