Section 335.1120  Procedures for Administrations Requiring a Written Directive

a)         For any administration requiring a written directive, the licensee shall develop, implement, and maintain written procedures to provide high confidence that:

1)         The patient's or human research subject's identity is verified before each administration; and

2)         Each administration is in accordance with the written directive.

b)         At a minimum, the procedures required by subsection (a) of this Section shall

address the following items that are applicable to the licensee's use of radioactive material:

1)         Verifying the identity of the patient or human research subject;

2)         Verifying that the administration is in accordance with the treatment plan, if applicable, and the written directive;

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 by Section 335.8010 of this Part.

c)         A licensee shall retain a copy of the procedures required by subsection (a) of this Section for the duration of the license.

(Source:  Added at 30 Ill. Reg. 9029, effective April 28, 2006)