[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: 10CFR35.29]

[Page 560]
 
                            TITLE 10--ENERGY
 
                CHAPTER I--NUCLEAR REGULATORY COMMISSION
 
PART 35--MEDICAL USE OF BYPRODUCT MATERIAL--Table of Contents
 
             Subpart B--General Administrative Requirements
 
Sec. 35.29  Administrative requirements that apply to the provision of mobile nuclear medicine service.

    (a) The Commission will license mobile nuclear medicine service only 
in accordance with subparts D, E and H of this part and Sec. 31.11 of 
this chapter.
    (b) Mobile nuclear medicine service licensees shall obtain a letter 
signed by the management of each client for which services are rendered 
that authorizes use of byproduct material at the client's address of 
use. The mobile nuclear medicine service licensee shall retain the 
letter for three years after the last provision of service.
    (c) If a mobile nuclear medicine service provides services that the 
client is also authorized to provide, the client is responsible for 
assuring that services are conducted in accordance with the regulations 
in this chapter while the mobile nuclear medicine service is under the 
client's direction.
    (d) A mobile nuclear medicine service may not order byproduct 
material to be delivered directly from the manufacturer or distributor 
to the client's address of use.

[51 FR 36951, Oct. 16, 1986, as amended at 53 FR 19247, May 27, 1988]