(a) A licensee shall provide the Commission a copy of the board certification and the written attestation(s), signed by a preceptor, the Commission or Agreement State license, the permit issued by a Commission master material licensee, the permit issued by a Commission or Agreement State licensee of broad scope, the permit issued by a Commission master material license broad scope permittee, or documentation that only accelerator-produced radioactive materials, discrete sources of radium-226, or both, were used for medical use or in the practice of nuclear pharmacy at a Government agency or Federally recognized Indian Tribe before November 30, 2007 or at all other locations of use before August 8, 2009, or an earlier date as noticed by the NRC, and for each individual no later than 30 days after the date that the licensee permits the individual to work as an authorized user, an authorized nuclear pharmacist, or an authorized medical physicist, under Sec. 35.13(b). For individuals permitted to work under Sec. 35.13(b)(4), within the same 30-day time frame, the licensee shall also provide, as appropriate, verification of completion of;
(1) Any additional case experience required in Sec. 35.390(b)(1)(ii)(G) for an authorized user under Sec. 35.300;
(2) Any additional training required in Sec. 35.690(c) for an authorized user under Sec. 35.600; and
(3) Any additional training required in Sec. 35.51(c) for an authorized medical physicist.
(b) A licensee shall notify the Commission no later than 30 days after:
(1) An authorized user, an authorized nuclear pharmacist, a Radiation Safety Officer, or an authorized medical physicist permanently discontinues performance of duties under the license or has a name change;
(2) The licensee permits an authorized user or an individual qualified to be a Radiation Safety Officer, under Sec. Sec. 35.50 and 35.59, to function as a temporary Radiation Safety Officer and to perform the functions of a Radiation Safety Officer in accordance with Sec. 35.24(c).
(3) The licensee's mailing address changes;
(4) The licensee's name changes, but the name change does not constitute a transfer of control of the license as described in Sec. 30.34(b) of this chapter; or
(5) The licensee has added to or changed the areas of use identified in the application or on the license where byproduct material is used in accordance with either Sec. 35.100 or Sec. 35.200 if the change does not include addition or relocation of either an area where PET radionuclides are produced or a PET radioactive drug delivery line from the PET radionuclide/PET radioactive drug production area.
(c) The licensee shall send the documents required in this section to the appropriate address identified in Sec. 30.6 of this chapter. [67 FR 20370, Apr. 24, 2002, as amended at 68 FR 58805, Oct. 10, 2003; 70 FR 16361, Mar. 30, 2005; 71 FR 15008, Mar. 27, 2006; 72 FR 55931, Oct. 1, 2007]