In accordance
with the PRA and 5 CFR 1320 this collection of information is
cleared for one year. When preparing to resubmit this collection
for OMB review, NRC should carefully evaluate each information item
to determine its practical utility. When conducting this evaluation
the NRC should 1) bear in mind that the medical care industry has
extensive experience dealing with potentially dangerous substances,
and 2) demonstrate the usefulness of this information by showing
how NRC used the information collected in the past. The evaluation
should weigh the benefits of this collection to hospitols, their
employees and patients against the 419,929 hours of reporting
burden.
Inventory as of this Action
Requested
Previously Approved
08/31/1989
08/31/1989
05/31/1988
29,279
0
469
419,929
0
268,325
0
0
0
10 CFR PART 35 CONTAINS REQUIREMENTS
THAT APPLY TO NRC LICENSEES WHO ARE AUTHORIZED TO ADMINISTER
BYPRODUCT MATERIAL OR ITS RADIATION TO HUMANS FOR MEDICAL CARE. THE
INFORMATION IN THE REQUIRED REPORTS AND RECORDS IS USED BY THE NRC
TO MAKE LICENSING AND REGULATORY DECISIONS TO ENSUR PROTECTION OF
THE PUBLIC HEALTH AND SAFETY.
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.