[Code of Federal Regulations] [Title 10, Volume 1] [Revised as of January 1, 2001] From the U.S. Government Printing Office via GPO Access [CITE: 10CFR35.80] [Page 567-568] TITLE 10--ENERGY CHAPTER I--NUCLEAR REGULATORY COMMISSION PART 35--MEDICAL USE OF BYPRODUCT MATERIAL--Table of Contents Subpart C--General Technical Requirements Sec. 35.80 Technical requirements that apply to the provision of mobile nuclear medicine service. A licensee providing mobile nuclear medicine service shall: (a) Transport to each address of use only syringes or vials containing prepared radiopharmaceuticals or radiopharmaceuticals that are intended for reconstitution of radiopharmaceutical kits; (b) Bring into each address of use all byproduct material to be used and, before leaving, remove all unused byproduct material and all associated waste; (c) Secure or keep under constant surveillance and immediate control all byproduct material when in transit or at an address of use; (d) Check survey instruments and dose calibrators as described in Secs. 35.50 and 35.51, and check all other transported equipment for proper function before medical use at each address of use; (e) Carry a radiation detection survey meter in each vehicle that is being used to transport byproduct material, and, before leaving a client address of use, survey all radiopharmaceutical areas of use with a radiation detection survey meter to ensure that all radiopharmaceuticals and all associated waste have been removed; (f) Retain a record of each survey required in paragraph (e) of this section for three years. The record must include the date of the survey, a plan of each area that was surveyed, the measured dose rate at several points in each area of use expressed in millirem per hour, the instrument used to make the [[Page 568]] survey, and the initials of the individual who performed the survey. [51 FR 36951, Oct. 16, 1986, as amended at 53 FR 19247, May 27, 1988]