82 FR 22836 - Agency Information Collection Activities: Proposed Collection: Public Comment Request; Information Collection Request Title: Scientific Registry of Transplant Recipients Information Collection Effort for Potential Donors for Living Organ Donation-New
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Health Resources and Services Administration Federal Register Volume 82, Issue 95 (May 18, 2017)
Health Resources and Services Administration
Federal Register Volume 82, Issue 95 (May 18, 2017)
| Page Range | 22836-22837 | |
| FR Document | 2017-10040 |
[Federal Register Volume 82, Number 95 (Thursday, May 18, 2017)] [Notices] [Pages 22836-22837] From the Federal Register Online [www.thefederalregister.org] [FR Doc No: 2017-10040] ----------------------------------------------------------------------- DEPARTMENT OF HEALTH AND HUMAN SERVICES Health Resources and Services Administration Agency Information Collection Activities: Proposed Collection: Public Comment Request; Information Collection Request Title: Scientific Registry of Transplant Recipients Information Collection Effort for Potential Donors for Living Organ Donation--New AGENCY: Health Resources and Services Administration (HRSA), Department of Health and Human Services (HHS). ACTION: Notice. ----------------------------------------------------------------------- SUMMARY: In compliance with the requirement for opportunity for public comment on proposed data collection projects of the Paperwork Reduction Act of 1995, HRSA announces plans to submit an Information Collection Request (ICR), described below, to the Office of Management and Budget (OMB). Prior to submitting the ICR to OMB, HRSA seeks comments from the public regarding the burden estimate, below, or any other aspect of the ICR. DATES: Comments on this ICR should be received no later than July 17, 2017. ADDRESSES: Submit your comments to [email protected] or mail the HRSA Information Collection Clearance Officer, Room 14N39, 5600 Fishers Lane, Rockville, MD 20857. FOR FURTHER INFORMATION CONTACT: To request more information on the proposed project or to obtain a copy of the data collection plans and draft instruments, email [email protected] or call the HRSA Information Collection Clearance Officer at (301) 443-1984. SUPPLEMENTARY INFORMATION: When submitting comments or requesting information, please include the information request collection title for reference, pursuant to Section 3506(c)(2)(A), the Paperwork Reduction Act of 1995. Information Collection Request Title: Scientific Registry of Transplant Recipients Information Collection Effort for Potential Donors for Living Organ Donation--New. Abstract: The Scientific Registry of Transplant Recipients (SRTR) is administered under contract with HRSA, an agency of HHS. HHS is authorized to establish and maintain mechanisms to evaluate the long- term effects associated with living donations (42 U.S.C. 273a) and is required to submit to Congress an annual report on the long-term health effects of living donation (42 U.S.C. 273b). The SRTR contractor will establish a pilot living donor registry in which 14 transplant programs will register all potential living donors who provide informed consent to participate in the pilot registry. The SRTR's authority to collect information concerning potential living donors is set forth in the Organ Procurement and Transplantation Network final rule requiring Organ Procurement Organizations and transplant hospitals to submit to the SRTR, as appropriate, information regarding ``donors of organs'' and ``other information that the Secretary deems appropriate'' 42 CFR 121.11(b)(2). Need and Proposed Use of the Information: The transplant programs will submit health information collected at the time of donation evaluation through a secure web-based data collection tool developed by the contractor. The SRTR contractor will maintain contact with registry participants and collect data on long-term health outcomes through surveys. The data collection will also include outcomes of evaluation including reasons for non-donation. The goal of the pilot registry is to develop data collection tools and survey instruments that can be used to expand the registry to include most, if not all, living donor transplant programs in the United States over time. Monitoring and reporting of long-term health outcomes of living donors post donation will provide useful information to transplant programs in their future donor selection process and will aid potential living donors in their decision to pursue living donation. Likely Respondents: Potential living donors, transplant programs, medical and scientific organizations, and public organizations. Burden Statement: Burden in this context means the time expended by persons to generate, maintain, retain, disclose, or provide the information requested. This includes the time needed to: (1) Review instructions; develop, acquire, install, and utilize technology and systems for the purpose of collecting, validating, and verifying information, processing and maintaining information, and disclosing and providing information; (2) train personnel to respond to a request for collection of information; (3) search data sources; (4) complete and review the collection of information; and (5) to transmit or otherwise disclose the information. The total annual burden hours estimated for this Information Collection Request are summarized in the table below. Total Estimated Annualized Burden Hours ---------------------------------------------------------------------------------------------------------------- Average number Average burden Form name Number of of responses Total number per response Total burden respondents per respondent of responses (in hours) hours ---------------------------------------------------------------------------------------------------------------- Potential Living Donor 14 55 770 1 770 Registration form.............. Potential Living Donor Follow-up 776 1 776 .50 388 form........................... ------------------------------------------------------------------------------- Total....................... * 790 .............. 1,546 .............. 1,158 ---------------------------------------------------------------------------------------------------------------- * Number of respondents for potential living donor registration forms is based on the number of programs participating in the pilot registry. Number of respondents for potential living donor follow-up forms is based on the number of potential living donors evaluated at the 14 participating programs in 2015. HRSA specifically requests comments on (1) the necessity and utility of the proposed information collection for the proper performance of the agency's functions; (2) the accuracy of the estimated burden; (3) ways to enhance the quality, utility, and clarity of the information to be collected; and (4) the use of automated collection techniques or other forms of information [[Page 22837]] technology to minimize the information collection burden. Jason E. Bennett, Director, Division of the Executive Secretariat. [FR Doc. 2017-10040 Filed 5-17-17; 8:45 am] BILLING CODE 4165-15-P
![22836 Federal Register / Vol. 82, No. 95 / Thursday, May 18, 2017 / Notices
Dated: May 15, 2017. FOR FURTHER INFORMATION CONTACT: To at the time of donation evaluation
William N. Parham, III, request more information on the through a secure web-based data
Director, Paperwork Reduction Staff, Office proposed project or to obtain a copy of collection tool developed by the
of Strategic Operations and Regulatory the data collection plans and draft contractor. The SRTR contractor will
Affairs. instruments, email paperwork@hrsa.gov maintain contact with registry
[FR Doc. 2017–10085 Filed 5–17–17; 8:45 am] or call the HRSA Information Collection participants and collect data on long-
BILLING CODE 4120–01–P Clearance Officer at (301) 443–1984. term health outcomes through surveys.
SUPPLEMENTARY INFORMATION: When The data collection will also include
submitting comments or requesting outcomes of evaluation including
DEPARTMENT OF HEALTH AND information, please include the reasons for non-donation. The goal of
HUMAN SERVICES information request collection title for the pilot registry is to develop data
reference, pursuant to Section collection tools and survey instruments
Health Resources and Services 3506(c)(2)(A), the Paperwork Reduction that can be used to expand the registry
Administration Act of 1995. to include most, if not all, living donor
Information Collection Request Title: transplant programs in the United States
Agency Information Collection Scientific Registry of Transplant over time. Monitoring and reporting of
Activities: Proposed Collection: Public Recipients Information Collection Effort long-term health outcomes of living
Comment Request; Information for Potential Donors for Living Organ donors post donation will provide
Collection Request Title: Scientific Donation—New. useful information to transplant
Registry of Transplant Recipients Abstract: The Scientific Registry of programs in their future donor selection
Information Collection Effort for Transplant Recipients (SRTR) is process and will aid potential living
Potential Donors for Living Organ administered under contract with donors in their decision to pursue living
Donation—New HRSA, an agency of HHS. HHS is donation.
authorized to establish and maintain
AGENCY: Health Resources and Services Likely Respondents: Potential living
mechanisms to evaluate the long-term
Administration (HRSA), Department of donors, transplant programs, medical
effects associated with living donations
Health and Human Services (HHS). and scientific organizations, and public
(42 U.S.C. 273a) and is required to
organizations.
ACTION: Notice. submit to Congress an annual report on
the long-term health effects of living Burden Statement: Burden in this
SUMMARY: In compliance with the donation (42 U.S.C. 273b). The SRTR context means the time expended by
requirement for opportunity for public contractor will establish a pilot living persons to generate, maintain, retain,
comment on proposed data collection donor registry in which 14 transplant disclose, or provide the information
projects of the Paperwork Reduction Act programs will register all potential requested. This includes the time
of 1995, HRSA announces plans to living donors who provide informed needed to: (1) Review instructions;
submit an Information Collection consent to participate in the pilot develop, acquire, install, and utilize
Request (ICR), described below, to the registry. The SRTR’s authority to collect technology and systems for the purpose
Office of Management and Budget information concerning potential living of collecting, validating, and verifying
(OMB). Prior to submitting the ICR to donors is set forth in the Organ information, processing and
OMB, HRSA seeks comments from the Procurement and Transplantation maintaining information, and disclosing
public regarding the burden estimate, Network final rule requiring Organ and providing information; (2) train
below, or any other aspect of the ICR. Procurement Organizations and personnel to respond to a request for
transplant hospitals to submit to the collection of information; (3) search data
DATES: Comments on this ICR should be sources; (4) complete and review the
SRTR, as appropriate, information
received no later than July 17, 2017. collection of information; and (5) to
regarding ‘‘donors of organs’’ and ‘‘other
ADDRESSES: Submit your comments to information that the Secretary deems transmit or otherwise disclose the
paperwork@hrsa.gov or mail the HRSA appropriate’’ 42 CFR 121.11(b)(2). information. The total annual burden
Information Collection Clearance Need and Proposed Use of the hours estimated for this Information
Officer, Room 14N39, 5600 Fishers Information: The transplant programs Collection Request are summarized in
Lane, Rockville, MD 20857. will submit health information collected the table below.
TOTAL ESTIMATED ANNUALIZED BURDEN HOURS
Average Average
Total Total
Number of number of burden per
Form name number of burden
respondents responses per response
responses hours
respondent (in hours)
Potential Living Donor Registration form ............................. 14 55 770 1 770
Potential Living Donor Follow-up form ................................ 776 1 776 .50 388
Total .............................................................................. * 790 ........................ 1,546 ........................ 1,158
* Number of respondents for potential living donor registration forms is based on the number of programs participating in the pilot registry.
jstallworth on DSK7TPTVN1PROD with NOTICES
Number of respondents for potential living donor follow-up forms is based on the number of potential living donors evaluated at the 14 partici-
pating programs in 2015.
HRSA specifically requests comments functions; (2) the accuracy of the use of automated collection techniques
on (1) the necessity and utility of the estimated burden; (3) ways to enhance or other forms of information
proposed information collection for the the quality, utility, and clarity of the
proper performance of the agency’s information to be collected; and (4) the
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![Federal Register / Vol. 82, No. 95 / Thursday, May 18, 2017 / Notices 22837
technology to minimize the information SUPPLEMENTARY INFORMATION: When patients with HIV, (2) the number and
collection burden. submitting comments or requesting characteristics of clients who receive
information, please include the RWHAP-supported oral health services,
Jason E. Bennett,
information request collection title for (3) the types and frequency of the
Director, Division of the Executive Secretariat. reference, in compliance with Section provision of these services, (4) the non-
[FR Doc. 2017–10040 Filed 5–17–17; 8:45 am] 3506(c)(2)(A) of the Paperwork reimbursed costs of oral health care
BILLING CODE 4165–15–P Reduction Act of 1995. provided to patients living with HIV,
Information Collection Request Title: and (5) the scope of grant recipients’
Ryan White HIV/AIDS Program Part F community-based collaborations and
DEPARTMENT OF HEALTH AND Dental Services Report, OMB No. 0915– training of providers. In addition to
HUMAN SERVICES 0151—Extension. meeting the goal of accountability to
Health Resources and Services Abstract: The Dental Reimbursement Congress, clients, public and
Administration Program (DRP) and the Community- community groups, and the general
Based Dental Partnership Program public, information collected in the DSR
Agency Information Collection (CBDPP) under Part F of the Ryan White is critical for HRSA, state and local
Activities: Submission to OMB for HIV/AIDS Program (RWHAP) offer grantees, and individual providers to
Review and Approval; Public Comment funding to accredited dental schools help assess the status of existing HIV-
Request; Ryan White HIV/AIDS and other accredited dental education related health service delivery systems.
Program Part F Dental Services programs to support the provision of Likely Respondents: Accredited
Report, OMB No. 0915-0151— oral health services for people living schools of dentistry and other
Extension with HIV as well as the education and accredited dental education programs,
training of oral health providers in HIV such as dental hygiene programs or
AGENCY: Health Resources and Services oral health care. Institutions eligible for those sponsored by a school of
Administration (HRSA), Department of these RWHAP Part F funds are dentistry, a hospital, or a public or
Health and Human Services. accredited schools of dentistry and private institution that offers
ACTION: Notice. other accredited dental education postdoctoral training in the specialties
programs, such as dental hygiene of dentistry, advanced education in
SUMMARY: In compliance with the programs or those sponsored by a school general dentistry, or a dental general
Paperwork Reduction Act of 1995, of dentistry, a hospital, or a public or practice residency.
HRSA has submitted an Information private institution that offers Burden Statement: Burden in this
Collection Request (ICR) to the Office of postdoctoral training in the specialties context means the time expended by
Management and Budget (OMB) for of dentistry, advanced education in persons to generate, maintain, retain,
review and approval. Comments general dentistry, or a dental general disclose, or provide the information
submitted during the first public review practice residency. The Dental Services requested. This includes the time
of this ICR will be provided to OMB. Report (DSR) collects data on program needed to review instructions; to
OMB will accept further comments from information, client demographics, oral develop, acquire, install, and utilize
the public during the review and health services, funding, and training. technology and systems for the purpose
approval period. Awards are authorized under section of collecting, validating, and verifying
DATES: Comments on this ICR should be 2692(b) of the Public Health Service Act information, processing and
received no later than June 19, 2017. (42 U.S.C. 300ff–111(b)). maintaining information, and disclosing
ADDRESSES: Submit your comments, Need and Proposed Use of the and providing information; to train
including the ICR Title, to the desk Information: The primary purpose of personnel and to be able to respond to
officer for HRSA, either by email to collecting this information annually is a collection of information; to search
OIRA_submission@omb.eop.gov or by to verify applicant eligibility and data sources; to complete and review
fax to 202–395–5806. determine reimbursement amounts for the collection of information; and to
FOR FURTHER INFORMATION CONTACT: To DRP applicants, as well as to document transmit or otherwise disclose the
request a copy of the clearance requests the program accomplishments of CBDPP information. As this ICR is an extension,
submitted to OMB for review, email the grant recipients. This information also the total burden hours are unchanged.
HRSA Information Collection Clearance allows HRSA to learn about (1) the The total annual burden hours
Officer at paperwork@hrsa.gov or call extent of the involvement of dental estimated for this ICR are summarized
(301) 443–1984. schools and programs in treating in the table below.
TOTAL ESTIMATED ANNUALIZED BURDEN—HOURS
Average
Number of
Number of Total burden per Total burden
Form name Type of respondent responses per
respondents responses response hours
respondent (in hours)
Dental Services Report ....... DRP .................................... 56 1 56 45 2,520
CBDPP ............................... 12 1 12 35 420
jstallworth on DSK7TPTVN1PROD with NOTICES
Total ............................. ............................................. 68 ........................ 68 ........................ 2,940
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Document Created: 2017-05-18 01:20:38
Document Modified: 2017-05-18 01:20:38
| Category | Regulatory Information | |
| Collection | Federal Register | |
| sudoc Class | AE 2.7: GS 4.107: AE 2.106: | |
| Publisher | Office of the Federal Register, National Archives and Records Administration | |
| Section | Notices | |
| Action | Notice. | |
| Dates | Comments on this ICR should be received no later than July 17, 2017. | |
| Contact | To request more information on the proposed project or to obtain a copy of the data collection plans and draft instruments, email [email protected] or call the HRSA Information Collection Clearance Officer at (301) 443-1984. | |
| FR Citation | 82 FR 22836 |
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