SErIES IAEA HumAn HEAltH SErIES IAEA Hum
SErIES IAEA HumAn HEAltH SErIES IAEA Hum
SErIES IAEA HumAn HEAltH SErIES IAEA Hum
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2.4.2. Review<br />
The review process will utilize interviews, observations, documentation<br />
review and measurements, and will be carried out in line with the audit schedule.<br />
Sometimes the interviews, observations of work and documentary reviews<br />
provide sufficient evidence of the local practice meeting ‘good’ practice<br />
standards. Often, however, it is desirable to support these observations with the<br />
results of suitable measurements or tests. These measurements and tests should<br />
be carried out using appropriate methods and equipment independent of the host<br />
facility/institution. The purpose of the tests and measurements is to verify the<br />
technique and accuracy of the local methods, as well as the competence of the<br />
local staff.<br />
Some aspects of the audit process will be carried out by the whole audit<br />
team; others will be carried out by relevant members of the audit team. The audit<br />
report forms in Appendix IV, equipment-specific checklists in Annex III and<br />
worksheets for physics procedures in Annex IV should be used by the team<br />
members to guide and record their evaluations during the audit review. It should<br />
be expected that all aspects of the diagnostic service will be reviewed in some<br />
way.<br />
The review will cover all of the elements outlined in Sections 3–5, under<br />
the following headings:<br />
—Quality management procedures and infrastructure;<br />
—Patient related procedures;<br />
—Technical procedures.<br />
The review process and schedule of the audit visit are outlined in Appendix II.<br />
At the end of the review, the audit team will prepare a draft report to be<br />
presented at the exit briefing, using the supplied format (see Appendix III).<br />
The auditors are expected to comment on the extent to which the facility/<br />
institution has met the criteria for good practice as outlined in the guidelines. Any<br />
significant issues should be verified prior to documentation in the draft report. It<br />
is also appropriate to document positive findings regarding areas of good<br />
practice.<br />
The draft report should also include recommendations at two levels:<br />
(1) Recommendations in regard to minor or major problems potentially<br />
resolvable by the facility/institution;<br />
(2) Recommendations in regard to major problems that may require<br />
intervention from outside the facility/institution for resolution.<br />
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