(a)
Have successfully completed 80 hours of classroom and laboratory training,
applicable to the medical use of sodium iodide I-131 for procedures requiring a
written directive. The training must include:
1. Radiation physics and
instrumentation;
2. Radiation
protection;
3. Mathematics
pertaining to the use and measurement of radioactivity;
4. Chemistry of radioactive material for
medical use; and
5. Radiation
biology; and
(b) Have
work experience, under the supervision of an authorized user who meets the
requirements in Rules
64E-5.657,
64E-5.660
or
64E-5.662, F.A.C., NRC or equivalent Agreement State requirements. A
supervising authorized user, who meets the requirements in subsection
64E-5.660(2),
F.A.C., must also have experience in administering dosages as specified in
sub-sub-subparagraph
64E-5.660(2)(a)
2.g.(II), F.A.C. The work experience must involve the following:
1. Ordering, receiving, and unpacking
radioactive materials safely and performing the related radiation
surveys;
2. Performing quality
control procedures on instruments used to determine the activity of dosages and
performing checks for proper operation of survey meters;
3. Calculating, measuring, and safely
preparing patient or human research subject dosages;
4. Using administrative controls to prevent a
medical event involving the use of radioactive material;
5. Using procedures to contain spilled
radioactive material safely and using proper decontamination procedures;
and
6. Administering dosages to
patients or human research subjects, that includes at least 3 cases involving
the oral administration of greater than 1.22 gigabecquerels (33 millicuries) of
sodium iodide I-131; and
(c) Have obtained written attestation that
the individual has satisfactorily completed the requirements in paragraphs
64E-5.662(3)(a) and 64E-5.662(3)(b), F.A.C., of this section, and have
demonstrated the ability to function independently as an authorized user to
fulfill the radiation safety related duties for a medical use licensee
authorized under Rule
64E-5.626,
64E-5.627
or
64E-5.630,
F.A.C., that require written directives. Have obtained written attestation,
signed by a preceptor authorized user or a residency program director who
represents a consensus of residency program faculties (as long as at least one
member of the residency program faculty is an authorized individual in the same
category designated by the applicant seeking authorized status) who meets the
requirements in Rule
64E-5.657,
64E-5.660
or
64E-5.662, F.A.C., NRC or equivalent Agreement State requirements. A
preceptor authorized user, who meets the requirements in subsection
64E-5.660(2),
F.A.C., must also have experience in administering dosages as specified in
sub-sub-subparagraph
64E-5.660(2)(a)
2.g.(II), F.A.C.