Translation, QA and third-party review for Pharma and Healthcare industries are about 95% of my current working time. I serve to all stages of drug development and marketing, from non-clinical studies to postmarketing surveillance and pharmacovigilance, including investigator brochures, CT protocols, drug labeling, contracts, patient information sheets, ICFs, patient diaries, SmPCs, marketing authorization dossiers, certificates of analysis, compliance certificates. Plus linguistic validation