Medical and life‑science content demands absolute precision, regulatory awareness, and deep subject‑matter expertise. Every document—whether a clinical trial protocol, a medical device manual, a pharmacovigilance report, or patient‑facing material—must be translated with unwavering accuracy to safeguard public health and uphold strict international standards.
At medicaltranslations.gr, we support organizations across the entire healthcare ecosystem, from pharmaceutical companies and CROs to medical device manufacturers, biotech innovators, and healthcare providers. Our team combines linguistic excellence with scientific literacy, ensuring that every translation is not only linguistically accurate but also terminologically consistent, culturally appropriate, and scientifically reliable.
We follow industry‑specific guidelines and regulatory frameworks, helping clients maintain compliance with EMA, FDA, MDR, IVDR, and other global requirements. By integrating quality‑assurance workflows, expert review, and specialized terminology management, we help protect patient safety, streamline regulatory submissions, and enable seamless communication across markets.
Our mission is simple: to empower healthcare organizations with translations they can trust—every time, in every language, and for every stage of the product lifecycle.
medicaltranslations.gr 