(a) Has
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 the following:
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 Rule
64E-5.657,
64E-5.660,
64E-5.661 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.(I) or
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 less than or equal to 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-5.661(3)(a) and 64E-5.661(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 that
required a written directive under Rule
64E-5.626,
64E-5.627
or
64E-5.630,
F.A.C. 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,
64E-5.661 or
64E-5.662,
F.A.C., NRC or equivalent Agreement State requirements. A preceptor authorized
user, who meets the requirement 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.(I) or
64E-5.660(2)(a)
2.g.(II), F.A.C.