Notice2025-10093
Agency Information Collection Activities; Submission for OMB Review; Comment Request; Disclosure of Medical Evidence
Primary source
Metadata and text below are from the Federal Register, a public-domain U.S. government work. Always verify the official published version before relying on it for any legal matter.
Published
June 4, 2025
Issuing agencies
Labor Department
Abstract
The Department of Labor (DOL) is submitting this Office of Workers' Compensation Programs (OWCP)-sponsored information collection request (ICR) to the Office of Management and Budget (OMB) for review and approval in accordance with the Paperwork Reduction Act of 1995 (PRA). Public comments on the ICR are invited.
Full Text
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<title>Federal Register, Volume 90 Issue 106 (Wednesday, June 4, 2025)</title>
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[Federal Register Volume 90, Number 106 (Wednesday, June 4, 2025)]
[Notices]
[Pages 23714-23715]
From the Federal Register Online via the Government Publishing Office [<a href="http://www.gpo.gov">www.gpo.gov</a>]
[FR Doc No: 2025-10093]
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DEPARTMENT OF LABOR
Agency Information Collection Activities; Submission for OMB
Review; Comment Request; Disclosure of Medical Evidence
ACTION: Notice of availability; request for comments.
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SUMMARY: The Department of Labor (DOL) is submitting this Office of
Workers' Compensation Programs (OWCP)-sponsored information collection
request (ICR) to the Office of Management and Budget (OMB) for review
and approval in accordance with the Paperwork Reduction Act of 1995
(PRA). Public comments on the ICR are invited.
DATES: The OMB will consider all written comments that the agency
receives on or before July 7, 2025.
ADDRESSES: Written comments and recommendations for the proposed
information collection should be sent within 30 days of publication of
this notice to <a href="http://www.reginfo.gov/public/do/PRAMain">www.reginfo.gov/public/do/PRAMain</a>. Find this particular
information collection by selecting ``Currently under 30-day Review--
Open for Public Comments'' or by using the search function.
Comments are invited on: (1) whether the collection of information
is necessary for the proper performance of the functions of the
Department, including whether the information will have practical
utility; (2) the accuracy of the agency's estimates of the burden and
cost of the collection of information, including the validity of the
methodology and assumptions used; (3) ways to enhance the quality,
utility and clarity of the information collection; and (4) ways to
minimize the burden of the collection of information on those who are
to respond, including the use of automated collection techniques or
other forms of information technology.
FOR FURTHER INFORMATION CONTACT: Nicole Bouchet by telephone at 202-
693-0213, or by email at <a href="/cdn-cgi/l/email-protection#12565d5e4d4240534d4247505e5b5152767d7e3c757d64"><span class="__cf_email__" data-cfemail="81c5cecdded1d3c0ded1d4c3cdc8c2c1e5eeedafe6eef7">[email protected]</span></a>.
SUPPLEMENTARY INFORMATION: The Black Lung Benefits Act (BLBA), 30
U.S.C. 901 et seq., may require parties to exchange all medical
information about the miner they develop in connection with a claim for
benefits, including information parties do not intent to submit as
evidence in the claim. BLBA regulations help protect a miner's health,
assist unrepresented parties, and promote accurate benefit
determinations. The potential parties to a BLBA claim include the
benefits claimant, the responsible coal mine operator and its insurance
carrier, and the Director of OWCP. Under BLBA, a party of a party's
agent who receives medical information about the miner must send a copy
to all other parties within 30 days after receipt or, if a hearing
before an administrative law judge has already been scheduled, at least
20 days before the hearing. The exchanged information is entered into
the record of the claim only if a party submits it into evidence. For
additional substantive information about this ICR, see the related
notice published in the Federal Register on March 4, 2025 (90 FR
11191).
This information collection is subject to the PRA. A Federal agency
generally
[[Page 23715]]
cannot conduct or sponsor a collection of information, and the public
is generally not required to respond to an information collection,
unless the OMB approves it and displays a currently valid OMB Control
Number. In addition, notwithstanding any other provisions of law, no
person shall generally be subject to penalty for failing to comply with
a collection of information that does not display a valid OMB Control
Number. See 5 CFR 1320.5(a) and 1320.6.
DOL seeks PRA authorization for this information collection for
three (3) years. OMB authorization for an ICR cannot be for more than
three (3) years without renewal. The DOL notes that information
collection requirements submitted to the OMB for existing ICRs receive
a month-to-month extension while they undergo review.
Agency: DOL-OWCP.
Title of Collection: Disclosure of Medical Evidence.
OMB Control Number: 1240-0054.
Affected Public: Private Sector--Businesses or other for-profits.
Total Estimated Number of Respondents: 6,797.
Total Estimated Number of Responses: 6,797.
Total Estimated Annual Time Burden: 1,135 hours.
Total Estimated Annual Other Costs Burden: $16,041.
(Authority: 44 U.S.C. 3507(a)(1)(D))
Nicole Bouchet,
Senior PRA Analyst.
[FR Doc. 2025-10093 Filed 6-3-25; 8:45 am]
BILLING CODE 4510-26-P
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This is legal information, not legal advice. Laws vary by jurisdiction and change frequently. Always verify current law with official sources and consult a licensed attorney in your jurisdiction for advice on your specific situation.