In accordance
with the Paperwork Reduction Act and 5 CFR 1320, this collection is
approved through January 31, 1993. However, if EPA implements
information collection requirements related to the National
Emission Standards for Hazardous Air Pollutant for Radionuclides,
the NRC, after consulting with EPA, is required to report to OMB in
writing, within two months of EPA's action, whether or not there is
any duplication of information collections. If there is, the NRC
must describe the steps it is taking to reduce th duplicative
burden.
Inventory as of this Action
Requested
Previously Approved
01/31/1993
01/31/1993
01/31/1992
8,422,955
0
8,422,955
302,944
0
302,944
0
0
0
THIS AMENDMENT TO 10 CFR 35 WOULD
REQUIRE MEDICAL USE OF LICENSEES TO DEVELOP AND IMPLEMENT A BASIC
QUALITY ASSURANCE PROGRAM TO PREVENT ERRORS IN THE ADMINISTRATION
OF BYPRODUCT MATERIAL TO PATIENTS. THIS AMENDMENT ALSO CONTAINS
MODIFICATIONS TO THE EXISTING REPORTING AND RECORDKEEPING
REQUIREMENTS OF CERTAIN THERAPY OR DIAGNOSTIC EVENTS.
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.