ICH-GCP compliant translation for clinical trials, regulatory submissions, and pharmaceutical documentation.
A mistranslated informed consent form doesn’t just create a compliance issue — it puts patients at risk. A mistranslated protocol can compromise an entire study.
They know the difference between “adverse event” and “adverse reaction” — and why it matters to the FDA.
Quality system: Translation → independent review → QA check → client review → finalization. Every step documented for audit readiness.
Clinical trial translation is project-based due to the specialized expertise and quality controls required. Pricing depends on volume, language pairs, and turnaround requirements.
Typical range: $0.12–$0.20/word for clinical documents with full QA workflow.
Volume discounts available for multi-study programs. Translation memory reduces costs on recurring document types (protocol amendments, updated ICFs).
Contact us for a project-specific quote: [email protected] or upload your documents.
A clinical trial file gets a quote review. Eligible standard documents are $19.99 per page. A birth, marriage, divorce, academic, or police record of up to 4 pages is delivered within 24 hours of order confirmation on business days, or that document is free. ATA corporate member #M-189351.
