10 CFR 35 is being completely revised
to be more performance oriented. Part 35 contains requirements for
licensees to administer byproduct material to humans for medical
use. The information in the required reports, and records is used
by NRC to ensure that the health and safety of the public is pro-
tected and that the licensees' possession and use of byproduct
material is in compliance with the license and regulatory
requirements.
On behalf of this Federal agency, I certify that
the collection of information encompassed by this request complies
with 5 CFR 1320.9 and the related provisions of 5 CFR
1320.8(b)(3).
The following is a summary of the topics, regarding
the proposed collection of information, that the certification
covers:
(i) Why the information is being collected;
(ii) Use of information;
(iii) Burden estimate;
(iv) Nature of response (voluntary, required for a
benefit, or mandatory);
(v) Nature and extent of confidentiality; and
(vi) Need to display currently valid OMB control
number;
If you are unable to certify compliance with any of
these provisions, identify the item by leaving the box unchecked
and explain the reason in the Supporting Statement.