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.