Pharmaceutical documentation

Specialized pharmaceutical and life sciences translation

Where Scientific Precision Meets Regulatory Compliance

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.

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Scientific Precision

Expert translation by life sciences specialists with deep domain knowledge and terminology expertise.

Regulatory Compliance

All projects follow structured terminology management and strict quality control for submission-ready results.

Audit-Ready Quality

Accurate, consistent, audit-ready medical translation with comprehensive documentation and traceability.

Athens-based boutique agency

Expert Translation for Regulated Industries

We support pharmaceutical, biotech, and life sciences organizations with regulatory-compliant translation services designed for accuracy, consistency, and audit-readiness.

Our specialized pharmaceutical services

Service Portfolio

Regulatory Submissions

Regulatory-compliant translation of EU submissions and multi-module dossiers with precise terminology management.

Product Information

Translation of SmPCs, package leaflets (PILs), and labeling texts that meet strict regulatory standards.

Clinical Trial Documentation

Clinical trial documentation, protocols, and informed consent forms with absolute accuracy and consistency.

Pharmacovigilance & MAH

Pharmacovigilance and MAH documentation with audit-ready quality and terminology precision.

Patient-Facing Materials

Patient-facing and medical materials that balance accuracy with accessibility and clarity.

Our quality commitment

Our Quality Process (TEP)

Every project undergoes a three-step review to ensure accurate, consistent, audit-ready medical translation.

1

Specialist Translation

by life sciences experts

2

Independent Review

Four-Eyes Principle verification

3

Final Quality Assurance

formatting, consistency, regulatory alignment

Why choose us

Secure. Consistent. Submission-Ready.

Because pharmaceutical translation is not just about language β€” it is about precision, compliance, and trust.

Harmonized Terminology

Harmonized terminology across regulatory and clinical documentation ensures consistency and compliance.

Submission Consistency

Consistency between submissions and updates with CAT tools, translation memories, and project glossaries.

Secure Workflows

Encrypted, GDPR-compliant workflows protect sensitive data and maintain regulatory standards.

Our commitment

Accuracy in Every Term

We ensure confidence in every submission through rigorous quality control and domain expertise.

GDPR-Compliant Workflows
Harmonized Terminology
CAT Tools & Translation Memories
Audit-Ready Quality

Ready to discuss your pharmaceutical translation project?

Confidence in Every Submission

Whether it's regulatory submissions, clinical trial documentation, or patient-facing materials, we have the expertise to deliver excellence.

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