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After having worked for 20 years in the Greek Pharma Market (Sales, Medical, Regulatory Affairs), I am currently working as a freelance Regulatory Affairs Consultant and Pharma/Medical Translator since Oct 2013.
My long translation experience includes Pharma/Medical product information documents (SmPCs, labeling, patient information leaflets), educational materials, clinical trial protocols, training materials etc.
Due to my solid Regulatory Affairs background, I am always up-to-date with current EU and Greek Regulatory requirements for the above mentioned documents (i.e. EU QRD templates/annexes, EDQM, MedDRA etc.)
Keywords: English, Greek, Regulatory Affairs, Pharmacovigilance (PV), Clinical Trials, Marketing, Pharma Market, EU QRD templates/annexes, Product Information, SmPC. See more.English, Greek, Regulatory Affairs, Pharmacovigilance (PV), Clinical Trials, Marketing, Pharma Market, EU QRD templates/annexes, Product Information, SmPC, Labeling, Patient Information Leaflet, Clinical Study Protocol, Pharma Educational Material, Patient Informed Consent Forms. See less.
