I am a Biologist, MSc with 4 years of Regulatory Medical Writing experience. I offer pharmaceutical translation services for the last 3 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 and Promotion Material.