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Pharmaceutical & Medical Translation

Specialized translation of pharmaceutical documentation, clinical trial protocols, patient information leaflets and medical device manuals from/into English, German, Czech, Ukrainian and other languages

We provide specialized translation of pharmaceutical, clinical and medical documentation starting from 295 CZK per standard page (1,800 characters including spaces). We ensure strict adherence to international regulatory standards, EMA terminology templates and validated medical glossaries. The exact price and turnaround time depend on the language combination, volume and file format. Send us an inquiry and we will prepare a quotation for your project. See our pricing page for more information.

Documents We Translate

  • Regulatory Submissions & Drug Registration – Summaries of Product Characteristics (SmPC / SPC), Patient Information Leaflets (PIL), labeling and outer packaging text, Marketing Authorization Applications (MAA) and regulatory variations
  • Clinical Trial Documentation – Clinical Trial Protocols (CTP), Informed Consent Forms (ICF), Investigator’s Brochures (IB), Clinical Study Reports (CSR), Case Report Forms (CRF / eCRF) and patient recruitment materials
  • Pharmacovigilance & Safety Documentation – Adverse Event (AE) reports, Periodic Safety Update Reports (PSUR), Periodic Benefit-Risk Evaluation Reports (PBRER), safety narratives and CIOMS forms
  • Medical Devices & Diagnostics (MDR / IVDR) – Instructions for Use (IFU), operating and maintenance manuals for medical equipment, Technical Documentation files, Declarations of Conformity (CE marking) and Notified Body submissions
  • Clinical Evaluation & Validation Reports – Clinical Evaluation Reports (CER), validation protocols, analytical method validations, stability study reports and Certificates of Analysis (CoA)
  • Patient-Facing Materials (eCOA / ePRO) – patient diaries, Patient-Reported Outcome (PRO) forms, Quality of Life (QoL) questionnaires, study cards and patient information brochures
  • Pharmaceutical Research & Development (CMC) – Chemistry, Manufacturing and Controls (CMC) documentation, preclinical and non-clinical study reports, toxicology summaries and scientific publications

How It Works

Send your documents

Send your files by email or through our contact form, specifying target languages, formatting requirements and preferred deadline.

Quote & turnaround time

We assess document volume, complexity and regulatory requirements, then provide an exact quotation and estimated delivery time.

Translation & quality review

A qualified translator translates using approved terminology and regulatory templates, followed by rigorous quality assurance review.

Delivery

We deliver the completed translation in your requested format within the agreed timeframe. Professional DTP typesetting and layout adjustment are also available upon request.