Clinical Translation – Precision in Every Word, Accuracy in Every Market

New Leads

QUALIFIED Pipeline

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More likely to bUY

Clinical translation isn’t just about language—it’s about patient safety, regulatory compliance, and medical precision. From clinical trial documentation to patient-reported outcomes (PROs), every word must be linguistically validated and culturally adapted to ensure accuracy, consistency, and compliance with global health regulations. With a specialized team of medical linguists, AI-driven quality control, and deep regulatory expertise, we help pharmaceutical companies, CROs, and healthcare providers communicate effectively across languages—without compromising on precision.

Why Clinical Translation Requires More Than Just Language Skills

Linguistic Validation for Global Consistency

We go beyond basic translation to ensure medical terminology, patient instructions, and trial documentation retain meaning across all languages and geographies.

  • Improves patient comprehension​
  • Reduces trial discrepancies​
  • Supports global data pooling and consistency

Regulatory Compliance for Global Health Standards

Every clinical document must comply with strict international regulations. Our regulatory specialists and medical linguists ensure that translations meet the highest industry standards, including:

  • ICH-GCP (International Council for Harmonisation – Good Clinical Practice)
  • FDA (U.S. Food and Drug Administration)
  • EMA (European Medicines Agency)
  • MHRA (UK Medicines and Healthcare Products Regulatory Agency)

AI-Driven Quality Control for Faster, More Accurate Translations

We integrate AI and human expertise to enhance clinical translation accuracy while reducing turnaround times. Our quality assurance process includes:

  • AI-powered terminology management for consistency
  • Bilingual clinical experts reviewing critical documentation
  • Automated QA checks for regulatory adherence

End-to-End Clinical Translation Services

We provide comprehensive clinical translation solutions, including:

  • Clinical trial protocols & investigator brochures
  • Informed consent forms (ICFs)
  • Patient-reported outcomes (PROs) & Quality of Life (QoL) questionnaires
  • Regulatory submissions & pharmacovigilance reports
  • Medical device labeling & instructions for use (IFUs)