[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: 10CFR35.410]

[Page 572]
 
                            TITLE 10--ENERGY
 
                CHAPTER I--NUCLEAR REGULATORY COMMISSION
 
PART 35--MEDICAL USE OF BYPRODUCT MATERIAL--Table of Contents
 
                  Subpart G--Sources for Brachytherapy
 
Sec. 35.410  Safety instruction.

    (a) The licensee shall provide radiation safety instruction to all 
personnel caring for the patient or the human research subject 
undergoing implant therapy. To satisfy this requirement, the instruction 
must describe:
    (1) Size and appearance of the brachytherapy sources;
    (2) Safe handling and shielding instructions in case of a dislodged 
source;
    (3) Procedures for patient or human research subject control;
    (4) Procedures for visitor control; and
    (5) Procedures for notification of the Radiation Safety Officer if 
the patient or the human research subject dies or has a medical 
emergency.
    (b) A licensee shall retain for three years a record 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 61785, Dec. 2, 1994]