Evaluate process equipment and manufacturing systems used in sterile product manufacturing, including equipment qualification records, operating parameters, alarms, controls, maintenance/calibration records, and associated procedures, and assess their potential impact on product quality, data integrity, and sterility assurance. Including URS, IQ, OQ, PQ, commissioning documentation, protocols, reports, deviations, and associated change controls, to determine whether equipment and processes were appropriately qualified and remain in a validated state.