Full-time freelance translator specialising in clinical trial documentation, including information for subjects, informed consent forms, protocols, ethics committee correspondence and safety reporting (adverse events and adverse drug reactions) Pharmaceutical regulatory affairs, including applications for marketing authorisation, renewals and variations (BfArM and Swissmedic) Use of EMA-QRD templates, appendices and reference documents to translate Summaries of Product Characteristics, Patient Information Leaflets and labelling textsCardiology, particularly stent implantation and aortic valve replacement procedures, and haematology, particularly leukaemia and stem cell transplants Hospital reports and discharge summaries
Medical journal articles
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