Medical Writing

After originally specialising in Regulatory Affairs and Pharmacovigilance within the Veterinary Pharmaceuticals Industry, and having overseen Clinical Trials and Clinical Trials Applications for veterinary species, I am now diversifying into the wider world of Medical Writing. This will include Regulatory, Medical Communications and Clinical Trials Writing for human vaccines, pharmaceuticals and medical devices, while keeping up to speed with all aspects of veterinary medicines.

With this in mind, I am studying for the EMWA Professional Development Programme Foundation Certificate. With four out of eight modules successfully completed at the Lisbon Conference in 2010: ‘Publication Planning’, ‘Targeting Your Audience’, ‘Subject Narratives for Clinical Study Reports’, ‘From Protocol to Study Report: What’s In Between?’, I have two modules in progress to be completed following the London Conference this month: ‘Basic Epidemiology for Medical Communicators’ and ‘The Patient Information Leaflet’ along with the not-for-credit module on ‘Publication Ethics’.

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