[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: 10CFR35.310]

[Page 570]
 
                            TITLE 10--ENERGY
 
                CHAPTER I--NUCLEAR REGULATORY COMMISSION
 
PART 35--MEDICAL USE OF BYPRODUCT MATERIAL--Table of Contents
 
               Subpart F--Radiopharmaceuticals for Therapy
 
Sec. 35.310  Safety instruction.

    (a) A licensee shall provide radiation safety instruction for all 
personnel caring for the patient or the human research subject receiving 
radiopharmaceutical therapy and hospitalized for compliance with 
Sec. 35.75 of this chapter. To satisfy this requirement, the instruction 
must describe the licensee's procedures for:
    (1) Patient or human research subject control;
    (2) Visitor control;
    (3) Contamination control;
    (4) Waste control; and
    (5) Notification of the Radiation Safety Officer in case of the 
patient's or the human research subject's death or medical emergency.
    (b) A licensee shall keep for three years a list of individuals 
receiving instruction required by paragraph (a) of this section, a 
description of the instruction, the date of instruction, and the name of 
the individual who gave the instruction.

[51 FR 36951, Oct. 16, 1986, as amended at 53 FR 19247, May 27, 1988; 59 
FR 61784, Dec. 2, 1994]