Online Application Order Form
for Products from the Healthcare Cost and Utilization Project
(HCUP)
Reinstatement with change of a previously approved collection
No
Regular
09/10/2025
Requested
Previously Approved
36 Months From Approved
1,800
0
1,050
0
51,250
0
To support AHRQ's mission to improve
health care through scientific research, HCUP databases and
software tools are disseminated to users outside of the Agency
through a mechanism known as the HCUP Central Distributor. The HCUP
Central Distributor assists qualified researchers to access uniform
research data across multiple states with the use of one
application process. The HCUP databases disseminated through the
Central distributor are referred to as "restricted access public
release files"; that is, they are publicly available, but only
under restricted conditions. The HCUP Central Distributor Online
Reporting System facilitates the HCUP data users with ordering,
purchasing, and re-using HCUP databases, including data
applications, requesting complementary databases, submitting data
re-use and data sharing requests. The website can be found at:
https://cdors.ahrq.gov/ The HCUP Central Distributor User Guide
provides detailed instructions on how to purchase, protect, re-use
and share the HCUP data. This ICR is for the activities associated
with the HCUP database application process not the collection of
health care data for HCUP databases. Revisions to this ICR include
a redesigned HCUP application form and reducing the number of DUAs
to one state and one nationwide version.
US Code:
42
USC 299 Name of Law: Healthcare Research and Quality Act of
1999
There have been no changes in
public use of the system (i.e., the number of respondents), however
there is an increase in the burden hours with this ICR, from 900 to
1,050 hours. This increase in burden is due to a more accurate
accounting of the burden associated with the individual steps in
the ordering process.
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.