I mostly deal with such documents: Clinical Trial Protocols and Informed Consent Forms, Instructions for Use (IFUs), Registration Dossiers for Medicines (SmPCs, packaging texts), Patient Guides, Patient Questionnaires, Doctor Guides, Investigator Brochures, Synopses, Training Documentation, CMC documentation, Medical Software, Case Study Report Forms, Clinical Study Report Forms, Patient Diaries, Preclinical - Phase IV Documentation, Case Report Forms (CRFs)