[Code of Federal Regulations]
[Title 10, Volume 1]
[Revised as of January 1, 2005]
From the U.S. Government Printing Office via GPO Access
[CITE: 10CFR35.10]

[Page 568]
 
                            TITLE 10--ENERGY
 
                CHAPTER I--NUCLEAR REGULATORY COMMISSION
 
PART 35_MEDICAL USE OF BYPRODUCT MATERIAL--Table of Contents
 
                      Subpart A_General Information
 
Sec. 35.10  Implementation.

    (a) A licensee shall implement the provisions in this part on or 
before October 24, 2002, with the exception of the requirements listed 
in paragraph (b) of this section.
    (b) A licensee shall implement the training requirements in 
Sec. Sec. 35.50(a), 35.51(a), 35.55(a), 35.59, 35.190(a), 35.290(a), 
35.390(a), 35.392(a), 35.394(a), 35.490(a), 35.590(a), and 35.690(a) on 
or before October 25, 2005.
    (c) Prior to October 25, 2005, a licensee shall satisfy the training 
requirements of this part for a Radiation Safety Officer, an authorized 
medical physicist, an authorized nuclear pharmacist, or an authorized 
user by complying with either:
    (1) The appropriate training requirements in subpart J; or
    (2) The appropriate training requirements in subpart B or subparts D 
through H.
    (d) If a license condition exempted a licensee from a provision of 
Part 35 on October 24, 2002, then the license condition continues to 
exempt the licensee from the requirements in the corresponding provision 
of Sec. Sec. 35.1-35.4002.
    (e) When a requirement in this part differs from the requirement in 
an existing license condition, the requirement in this part shall 
govern.
    (f) A licensee shall continue to comply with any license condition 
that requires it to implement procedures required by Sec. Sec. 35.610, 
35.642, 35.643, and 35.645 until there is a license amendment or renewal 
that modifies the license condition.

[67 FR 20370, Apr. 24, 2002, as amended at 69 FR 55737, Sept. 16, 2004]