I am a Biologist, MSc experienced in Regulatory Medical Writing. I offer pharmaceutical translation services for the last 10 years and have translated/edited Clinical Trial documents (Protocols, ICFs, Letters submitted to the Authorities, Clinical Trial Agreements), Product Information (Summary of Product Characteristics, Package Leaflets, Labelling), Medical Devices Manuals and Brochures, Research Articles, Press Releases, Global Value Dossiers, Promotion Material, Academic Books, etc.