Research

Records that document the permission of persons willing to donate their body for scientific study. File may include registration record, correspondence, and other related records.

Records that document the use of hazardous carcinogenic compounds by university researchers. File may include research protocols; applications for use of Class B & C chemical carcinogens; chemical carcinogen animal care requirement records; lists of personnel involved in laboratory contact with chemical carcinogens; list of carcinogenic compounds to be used in the specific research project; correspondence; and other related records.

Research data and documentation gathered or created in the course of Phase IV of a clinical trial sponsored by an agency outside the University. May include case history records, case reports, study protocol and amendments, patient care data, objectives and purpose of the study, selection criteria, clinical procedures, FDA records, serious adverse events reports, study design and other documentation relating to study protocols. Does not include materials also maintained in official patient medical record.

Research data and documentation gathered or created in the course of a clinical trial in which Emory is the primary sponsor. May include case reports, shipment records, research data from investigators, internal research data, study protocols/designs and amendments, FDA records, and serious adverse events reports.