HRSA will use the information for the purpose of ensuring that providers who received over $750,000 in funding from any of the Provider Relief Program combined to 1) submit an audit per 45 CFR 75 Subpart F, 2) any documentation and attestation needed to resolve any audit findings, and 3) an attestation or documentation to prove an audit is not required. If the information is not collected, HRSA will not be in compliance with 45 CFR 75 Subpart F and will limit HRSAâs ability to monitor the Federal programs. In addition, HRSAâs ability to conduct delinquent audit follow-up on appropriate entities will be jeopardized if we cannot verify who has submitted their audit. There would be a harm to the public if this collection is not approved because HRSA would be delayed in following 45 CFR 75 Subpart F and recovering federal funds not utilized in accordance with the Provider Relief Program Terms and Conditions.
PL:
Pub.L. 116 - 260 0
Name of Law: Coronavirus Response and Relief Supplemental Appropriations
PL:
Pub.L. 116 - 136 0
Name of Law: Coronavirus Aid, Relief, and Economic Security (CARES) Act
PL:
Pub.L. 116 - 127 0
Name of Law: Families First Coronavirus Response Act
PL:
Pub.L. 117 - 2 0
Name of Law: American Rescue Plan Act of 2021
PL:
Pub.L. 116 - 139 0
Name of Law: Paycheck Protection Program (PPP) and Health Care Enhancement Act
The Delinquent Audit Follow-up General Email Blast that was included in the Emergency Clearance Package has been adjusted to provide additional clarification to providers about the audit requirements and include the attestation form, the average burden hours per response increased from 0.05 hours to 0.25 hours. As a result, the estimated burden for the Delinquent Audit Follow-up General Email Blast increased from 12,600 to 63,000, an increase of 50,400 respondents. The estimated burden for the entire collection increased from 388,975 to 439,375.
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.