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.