Federal Register - August 9, 2021
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Source: Federal Register
lotter on DSK11XQN23PROD with NOTICES1
Federal Register / Vol. 86, No. 150 / Monday, August 9, 2021 / Notices functions of the Advisory Board include providing advice on the development of probability of causation guidelines that have been promulgated by the Department of Health and Human Services HHS as a final rule; advice on methods of dose reconstruction, which have also been promulgated by HHS as a final rule; advice on the scientific validity and quality of dose estimation and reconstruction efforts being performed for purposes of the compensation program; and advice on petitions to add classes of workers to the Special Exposure Cohort SEC. In December 2000, the President delegated responsibility for funding, staffing, and operating the Advisory Board to HHS, which subsequently delegated this authority to CDC. NIOSH implements this responsibility for CDC.
The Advisory Boards charter was issued on August 3, 2001, renewed at appropriate intervals, and rechartered under Executive Order 13889 on March 22, 2020, and will terminate on March 22, 2022.
Purpose: The Advisory Board is charged with a providing advice to the Secretary, HHS, on the development of guidelines under Executive Order 13179; b providing advice to the Secretary, HHS, on the scientific validity and quality of dose reconstruction efforts performed for this program; and c upon request by the Secretary, HHS, advise the Secretary on whether there is a class of employees at any Department of Energy facility who were exposed to radiation but for whom it is not feasible to estimate their radiation dose, and on whether there is reasonable likelihood that such radiation doses may have endangered the health of members of this class.
SDRR was established to aid the Advisory Board in carrying out its duty to advise the Secretary, HHS, on dose reconstruction.
Matters To Be Considered: The agenda will include discussions on the following dose reconstruction program quality management and assurance activities: Dose reconstruction cases under review from Set 29, possibly including cases involving: Albuquerque Operations Office, Area IV of the Santa Susana Field Laboratory, Argonne National Laboratory-East, Argonne National Laboratory-West, Battelle Laboratories-King Avenue, Clarksville Modification Center, Feed Materials Production Center FMPC, Fermi National Accelerator Laboratory, General Atomics, Hanford, Idaho National Laboratory, Lawrence Berkeley National Laboratory, Lawrence Livermore National Laboratory, Los Alamos National Laboratory, Mound
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Plant, Nevada Test Site, Oak Ridge Gaseous Diffusion Plant K25, Oak Ridge Institute for Science and Education, Oak Ridge National Laboratory X10, Pacific Northwest National Laboratory, Paducah Gaseous Diffusion Plant, Pantex Plant, Portsmouth Gaseous Diffusion Plant, Rocky Flats Plant, Savannah River Site, and/or Y12 Plant. If time permits, there may also be discussion on professional judgement in response to the April 12, 2021 SDRR report to the Advisory Board. Agenda items are subject to change as priorities dictate.
The Director, Strategic Business Initiatives Unit, Office of the Chief Operating Officer, Centers for Disease Control and Prevention, has been delegated the authority to sign Federal Register notices pertaining to announcements of meetings and other committee management activities, for both the Centers for Disease Control and Prevention and the Agency for Toxic Substances and Disease Registry.
Kalwant Smagh, Director, Strategic Business Initiatives Unit, Office of the Chief Operating Officer, Centers for Disease Control and Prevention.
FR Doc. 202116954 Filed 8621; 8:45 am BILLING CODE 416318P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Community Living Agency Information Collection Activities; Proposed Collection; Public Comment Request; Centers for Independent Living Program Performance Report 09850061
Administration for Community Living, Health and Human Services HHS.
AGENCY:
ACTION:
Notice.
The Administration for Community Living ACL is announcing an opportunity for the public to comment on the proposed collection of information listed above. Under the Paperwork Reduction Act of 1995 the PRA, Federal agencies are required to publish a notice in the Federal Register concerning each proposed collection of information, including each proposed extension of an existing collection of information, and to allow 60 days for public comment in response to the notice. This Proposed Extension without Revision of a Currently Approved Collection ICR Ext solicits comments on the information collection requirements relating to the Centers for
SUMMARY:
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Independent Living under the Rehabilitation Act of 1973.
DATES: Comments on the collection of information must be submitted electronically by 11:59 p.m. EST or postmarked by October 8, 2021.
ADDRESSES: Submit electronic comments on the collection of information to: Peter Nye at OILPPRAComments@acl.hhs.gov.
Submit written comments on the collection of information to Administration for Community Living, Washington, DC 20201, Attention: Peter Nye.
FOR FURTHER INFORMATION CONTACT:
Peter Nye, Administration for Community Living, Washington, DC
20024, 202 7957606 or OILPPRAComments@acl.hhs.gov.
SUPPLEMENTARY INFORMATION: Under the PRA 44 U.S.C. 35013520, Federal agencies must obtain approval from the Office of Management and Budget OMB for each collection of information they conduct or sponsor.
Collection of information is defined in 44 U.S.C. 35023 and 5 CFR
1320.3c and includes agency requests or requirements that members of the public submit reports, keep records, or provide information to a third party.
Section 3506c2A of the PRA 44
U.S.C. 3506c2A requires Federal agencies to provide a 60-day notice in the Federal Register concerning each proposed collection of information, including each proposed extension of an existing collection of information, before submitting the collection to OMB
for approval. To comply with this requirement, ACL is publishing a notice of the proposed collection of information set forth in this document.
With respect to the following collection of information, ACL invites comments on our burden estimates or any other aspect of this collection of information, including:
1 Whether the proposed collection of information is necessary for the proper performance of ACLs functions, including whether the information will have practical utility;
2 the accuracy of ACLs estimate of the burden of the proposed collection of information, including the validity of the methodology and assumptions used to determine burden estimates; 3 ways to enhance the quality, utility, and clarity of the information to be collected; and 4 ways to minimize the burden of the collection of information on respondents, including through the use of automated collection techniques when appropriate, and other forms of information technology.
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