• clinical trials/pharmaceutical industry (CTAs, protocols, investigator CVs, IRB/IEC opinions, IBs, ICFs, patient information sheets, diaries, questionnaires, PROs, RA correspondence; analytical procedures, CoAs, CPPs, DMFs, GMP certificates, MIAs, PILs, PSURs, SMPCs, SOPs, labels, validation reports)
• medical devices (diagnostic/surgical tools, lab equipment)
• medical records (case records, certificates, diagnostic findings)
• public health (brochures, flyers, guides, leaflets, posters)