Approved for use
through 2/2002 under the following conditions: 1) Before placing
the instrument on the web, HCFA submits for OMB review: a) the
final computer screens and provides a live web site demonstration.
The revised instrument (and screens) should have a general
description of the characteristics of catalogue entries and should
include the critical screening questions as identified in this
clearance package at the beginning of the survey. The survey also
must incorporate skip patterns, as appropriate, to reduce burden on
the industry. At the beginning of the instrument, HCFA must explain
its privacy protections for proprietary information. In addition,
HCFA must allow for an unlimited number of references and
attachments of product testimonials. Finally, HCFA must reevaluate
the necessity of certain sensitive proprietary information such as
corporate revenues; b) a more detailed, technical plan for security
safeguards of proprietary information; and c) all promotional/press
materials encouraging participation in this "request for
information": and 2) the next submission for OMB must include a
general and item nonresponse analysis and recom- mendations for
enhancing vendor participation and reducing unnecessary
burden.
Inventory as of this Action
Requested
Previously Approved
02/28/2002
02/28/2002
450
0
0
1,350
0
0
0
0
0
This information collection tool is
essential to providing the Health Care Financing Administration
(HCFA) a vehicle to ascertain cutting edge fraud, waste, and abuse
detection products. HCFA and its contractors presently use a number
of these tools, as do other segments of Government, the health care
industry, and industry generally. New products taking advantage of
new technologies are in continuous development. This completely
voluntary survey will ensure that HCFA is vigilant in identifying
new advances to help fight the scourge of Medicare fraud and
abuse.
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.