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A.
For any administration requiring a written directive, a licensee must develop, implement, and maintain written procedures to provide high confidence that:
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(1)
the patient's or human research subject's identity is verified before each administration; and
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(2)
each administration is in accordance with the written directive.
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B.
At a minimum, the procedures required by item A must address the following that are applicable to the licensee's use of radioactive material:
§
(1)
verifying the identity of the patient or human research subject;
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(2)
verifying that the administration is in accordance with the treatment plan, if applicable, and the written directive;
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(3)
checking both manual and computer-generated dose calculations; and
§
(4)
verifying that any computer-generated dose calculations are correctly transferred into the consoles of therapeutic medical units authorized under part 4731.4404 or 4731.4463.