
In pharmaceutical and clinical environments, language is part of compliance. A single error in an SmPC, PIL, regulatory dossier, or clinical trial document can delay approvals or raise regulatory scrutiny.
Expert translation by life sciences specialists with deep domain knowledge and terminology expertise.
All projects follow structured terminology management and strict quality control for submission-ready results.
Accurate, consistent, audit-ready medical translation with comprehensive documentation and traceability.
Athens-based boutique agency
We support pharmaceutical, biotech, and life sciences organizations with regulatory-compliant translation services designed for accuracy, consistency, and audit-readiness.
Our specialized pharmaceutical services
Regulatory-compliant translation of EU submissions and multi-module dossiers with precise terminology management.
Translation of SmPCs, package leaflets (PILs), and labeling texts that meet strict regulatory standards.
Clinical trial documentation, protocols, and informed consent forms with absolute accuracy and consistency.
Pharmacovigilance and MAH documentation with audit-ready quality and terminology precision.
Patient-facing and medical materials that balance accuracy with accessibility and clarity.
Our quality commitment
Every project undergoes a three-step review to ensure accurate, consistent, audit-ready medical translation.
by life sciences experts
Four-Eyes Principle verification
formatting, consistency, regulatory alignment
Why choose us
Because pharmaceutical translation is not just about language β it is about precision, compliance, and trust.
Our commitment
We ensure confidence in every submission through rigorous quality control and domain expertise.
Ready to discuss your pharmaceutical translation project?
Whether it's regulatory submissions, clinical trial documentation, or patient-facing materials, we have the expertise to deliver excellence.