Working languages:
English to Greek
French to Greek
Greek to English

Savvas Georgiou
Expert Medical Translation

Limassol, Cyprus
Local time: 20:20 EET (GMT+2)

Native in: Greek Native in Greek
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I am a highly experienced Medical Translator, working exclusively in the translation of Medical, Pharmaceutical and Regulatory documentation with top-notch pharmaceutical multinationals, including GlaxoSmithKline and Novartis, translation agencies specializing in the medical -pharmaceutical sector and with international medical institutions and healthcare organisations.
As part of my services a post translation Quality Review is also performed on third party produced translations, in order to validate the terminology of the translated text in the target language and ensure the suitability of the medical writing style for publishing and official use.
Keywords: Medical Reports, Internal Medicine, Standard operating procedures (SOPs), Medical Certificates, Oncology, Validation Reports, Articles in Medical journals, Haematology, Toxicology, Medical Diplomas/Resumes, Immunology, Audit/ Inspection Reports, Patient Medical Records, Traumatology, GMP Certificates, Medical Practice Guidelines, Nutritional Healthcare, Certificates of analysis, Laboratory Tests & Reports, Endocrinology, Brand Promotional Materials, Imaging Reports (CT, MRI, PET), Pulmonology Sales Force Educational Trainingmaterials, Medical Device User Manuals, Dermatology, Product Monographs, Questionnaires & Surveys, Gynaecology, Drug Specifications, Patient Education materials, Obstetrics Manufacturing Protocols, Forensic Pathology reports Cosmetic surgery, Press Releases, HospitalDischarge Letters, Cardiology, Summary of product Characteristics (SmPCs), Medical Insurance contracts, Neurology, Patient Information Leaflets (PILs), Medical insurance claims, Urology, Labeling, Physician instructions, Biochemistry, Pharmaceutical correspondence, Laboratory diagnostic kits, Microbiology, Pharmaceutical patents, clinical trialProtocols & Amendments, adverse events Reports, Country specific Drug Registration Dossiers, Informed Consent Forms, Centralised and MR European applications, Case Report Forms PSURs, Investigational New Drug Applications, Patient Reported outcomes, Pharmacovigilance System Master Files, Common Technical Doc. (CTD) Modules, Investigational Drug safety Repor, individual case safety reports, Marketing Authorization Certificates, Quality of Life Questionnaires, Risk Management Plans, Marketing Authorization application forms, Investigator Brochures, Pharmacovigilance SOPs, Health supplements Registration, IRB/Ethics committee documents, Inspection/Audit Reports, Correspondence with Regulators, Drug safety Correspondence.

Profile last updated
Nov 3, 2015

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