I provide translation, proofreading/editing and quality management services regarding written texts on pharmaceuticals with 10 years of experience. Common document types that I work with include: EU documents, Clinical trial texts, Informed Consent Forms (ICF), drug registration dossiers, Ministry of Health correspondence, Good Manufacturing Practices (GMP), Summary of Product Characteristics (SPC), Patient Information Leaflets (PILs), case reports, scientific articles and theses.