Regulatory affairs (summaries of product characteristics, patient information leaflets, labelling)
Clinical trial documentation (protocol summaries, informed consent forms, product information, patient questionnaires, patient assessment instructions, clinical trials contracts etc.)
Optometrical texts and documents (lens fitting instructions, patient and optometrist information, marketing texts etc.)
Medical devices documentation (instructions for use etc.)
Proofreading, quality management, reconciliation of all types of medical texts mentioned above, linguistic validation of patient reported outcomes
Linguistic analysis, linguistic review
Translation of five books from the series Books Beyond Words on the subject of sexual abuse and depression in people with learning disabilities
