We have
reinstated approval for this ongoing collection and have recorded
the burden as a program change due to the long (three year) lapse
in approval.
Inventory as of this Action
Requested
Previously Approved
10/31/1997
10/31/1997
357
0
0
4,036
0
0
0
0
0
THESE FORMS WILL BE USED BY
INVESTIGATORS AND THEIR DESIGNEES (PHARMACISTS AND NURSES) TO TRACK
THE DISPENSING OF NCI-SPONSORED INVESTIGATIONAL NEW DRUGS UNDER NCI
CLINICAL PROTOCOLS. THESE FORMS WILL SERVE AS A LINK BETWEEN THE
NCI DRUG DISTRIBUTION DATA AND THE PROTOCOL PATIENT DATA TO ENSURE
THAT INVESTIGATIONAL DRUGS ARE BEING USED PROPERLY, IN ACCORDANCE
WITH THE NOTICE(S) OF CLAIMED
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.