AK1 |
Using a high‐quality dosimetry system calibrated against the local secondary standard, all beams and cones in use are recalibrated |
AK2 |
Timer and end‐effect error measurement may be performed in conjunction with AK3 |
AK3 |
Output linearity measurement for a clinically used filter/cone combination at a standard SSD and a dose range of 10−1000 cGy |
AK4 |
Output reproducibility verification for a clinically used filter/cone combination. These measurements should be repeated at typical tilt and head rotation used for treatments |
AK5 |
Output error when the beam is interrupted during the irradiation for a clinically used filter/cone combination |
AK6 |
The HVL of any clinically used beams is measured. The HVLs measured in millimeters of Al or millimeters of Cu as appropriate are compared with the values obtained at commissioning. These tolerances acknowledge measurement uncertainty |
AK7 |
Focal spot—quantitative measurement, assessed relative to acceptance test value where applicable |
AK8 |
Using a pin hole or resolution tool |
AK9 |
Verification of percentage depth dose measurements for all used filter/cone combinations against baseline |
AK10 |
Verification of inplane and crossplane profiles at different depths for all used filter/cone combinations against baseline |
AK11 |
To ensure redundancy and adequate monitoring, a second qualified medical physicist must independently verify the implementation, analysis, and interpretation of the quality control tests at least annually |