81 FR 24616 - Proposed Data Collection Submitted for Public Comment and Recommendations
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention Federal Register Volume 81, Issue 80 (April 26, 2016)
Centers for Disease Control and Prevention
Federal Register Volume 81, Issue 80 (April 26, 2016)
| Page Range | 24616-24618 | |
| FR Document | 2016-09657 |
[Federal Register Volume 81, Number 80 (Tuesday, April 26, 2016)] [Notices] [Pages 24616-24618] From the Federal Register Online [www.thefederalregister.org] [FR Doc No: 2016-09657] ----------------------------------------------------------------------- DEPARTMENT OF HEALTH AND HUMAN SERVICES Centers for Disease Control and Prevention [60Day-16-0199; Docket No. CDC-2016-0039] Proposed Data Collection Submitted for Public Comment and Recommendations AGENCY: Centers for Disease Control and Prevention (CDC), Department of Health and Human Services (HHS). ACTION: Notice with comment period. ----------------------------------------------------------------------- SUMMARY: The Centers for Disease Control and Prevention (CDC), as part of its continuing efforts to reduce public burden and maximize the utility of government information, invites the general public and other Federal agencies to take this opportunity to comment on proposed and/or continuing information collections, as required by the Paperwork Reduction Act of 1995. This notice invites comment on an extension request for the information collection entitled Application for Permit to Import Biological Agents and Vectors of Human Disease into the United States and Application for Permit to Import or Transport Live Bats (42 CFR 71.54). DATES: Written comments must be received on or before June 27, 2016. ADDRESSES: You may submit comments, identified by Docket No. CDC-2016- 0039 by any of the following methods:Federal eRulemaking Portal: Regulation.gov. Follow the instructions for submitting comments. Mail: Leroy A. Richardson, Information Collection Review Office, Centers for Disease Control and Prevention, 1600 Clifton Road, NE., MS-D74, Atlanta, Georgia 30329. Instructions: All submissions received must include the agency name and Docket Number. All relevant comments received will be posted without change to Regulations.gov, including any personal information provided. For access to the docket to read background documents or comments received, go to Regulations.gov. Please note: All public comment should be submitted through the Federal eRulemaking portal (Regulations.gov) or by U.S. mail to the address listed above. FOR FURTHER INFORMATION CONTACT: To request more information on the proposed project or to obtain a copy of [[Page 24617]] the information collection plan and instruments, contact the Information Collection Review Office, Centers for Disease Control and Prevention, 1600 Clifton Road, NE., MS-D74, Atlanta, Georgia 30329; phone: 404-639-7570; Email: [email protected]. SUPPLEMENTARY INFORMATION: Under the Paperwork Reduction Act of 1995 (PRA) (44 U.S.C. 3501-3520), Federal agencies must obtain approval from the Office of Management and Budget (OMB) for each collection of information they conduct or sponsor. In addition, the PRA also requires Federal agencies to provide a 60-day notice in the Federal Register concerning each proposed collection of information, including each new proposed collection, each proposed extension of existing collection of information, and each reinstatement of previously approved information collection before submitting the collection to OMB for approval. To comply with this requirement, we are publishing this notice of a proposed data collection as described below. Comments are invited on: (a) Whether the proposed collection of information is necessary for the proper performance of the functions of the agency, including whether the information shall have practical utility; (b) the accuracy of the agency's estimate of the burden of the proposed collection of information; (c) ways to enhance the quality, utility, and clarity of the information to be collected; (d) ways to minimize the burden of the collection of information on respondents, including through the use of automated collection techniques or other forms of information technology; and (e) estimates of capital or start- up costs and costs of operation, maintenance, and purchase of services to provide information. Burden means the total time, effort, or financial resources expended by persons to generate, maintain, retain, disclose or provide information to or for a Federal agency. This includes the time needed to review instructions; to 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; to train personnel and to be able to respond to a collection of information, to search data sources, to complete and review the collection of information; and to transmit or otherwise disclose the information. Proposed Project Application for Permit to Import Biological Agents and Vectors of Human Disease into the United States and Application for Permit to Import or Transport Live Bats (42 CFR 71.54) (OMB Control No. 0920- 0199, exp. 01/31/2017)--Extension--Office of Public Health Preparedness and Response (OPHPR), Centers for Disease Control and Prevention (CDC). Background and Brief Description Section 361 of the Public Health Service Act (42 U.S.C. 264), as amended, authorizes the Secretary of Health and Human Services to make and enforce such regulations as are necessary to prevent the introduction, transmission, or spread of communicable diseases from foreign countries into the States or possessions, or from one State or possession into any other State or possession. Part 71 of Title 42, Code of Federal Regulations (Foreign Quarantine) sets forth provisions to prevent the introduction, transmission, and spread of communicable disease from foreign countries into the United States. Subpart F-- Importations--contains provisions for the importation of infectious biological agents, infectious substances, and vectors (42 CFR 71.54); requiring persons that import these materials to obtain a permit issued by the CDC. CDC requests Office of Management and Budget approval to collect information for three years using the Application for Permit to Import Infectious Biological Agents into the United States and the Application for a Permit to Import or Transport Live Bats. The Application for Permit to Import Biological Agents, Infectious Substances and Vectors of Human Disease into the United States form is used by laboratory facilities, such as those operated by government agencies, universities, and research institutions to request a permit for the importation of biological agents, infectious substances, or vectors of human disease. This form currently requests applicant and sender contact information; description of material for importation; facility isolation and containment information; and personnel qualifications. CDC plans to make no changes to this application. The Application for Permit to Import or Transport Live Bats form is used by laboratory facilities such as those operated by government agencies, universities, research institutions, and for educational, exhibition, or scientific purposes to request a permit for the importation, and any subsequent distribution after importation, of live bats. This form currently requests the applicant and sender contact information; a description and intended use of bats to be imported; and facility isolation and containment information. CDC plans to make no changes to this application. Estimates of burden for the survey are based on information obtained from the CDC import permit database on the number of permits issued on annual basis since 2010. The total estimated burden for the one-time data collection is 545 hours. There are no costs to respondents except their time. Estimated Annualized Burden Hours ---------------------------------------------------------------------------------------------------------------- Average Number of Number burden per Total Type of respondent Form name respondents responses per response (in burden respondent hours) hours ---------------------------------------------------------------------------------------------------------------- Applicants Requesting to Import Application for 1,625 1 20/60 542 Biological Agents, Infectious Permit to Import Substances and Vectors. Biological Agents, Infectious Substances and Vectors of Human Disease into the United States. Applicants Requesting to Import Application for a 10 1 20/60 3 Live Bats. Permit to Import Live Bats. ---------------------------------------------------------- Total....................... ................... .............. .............. .............. 545 ---------------------------------------------------------------------------------------------------------------- [[Page 24618]] Leroy A. Richardson, Chief, Information Collection Review Office, Office of Scientific Integrity, Office of the Associate Director for Science, Office of the Director, Centers for Disease Control and Prevention. [FR Doc. 2016-09657 Filed 4-25-16; 8:45 am] BILLING CODE 4163-18-P
![24616 Federal Register / Vol. 81, No. 80 / Tuesday, April 26, 2016 / Notices
primary Federal agency for protecting During Phase 1, CDC will conduct 850 users. CDC will also pilot test and
health and promoting quality of life telephone interviews with 50 evaluate a direct technical assistance
through the prevention and control of individuals who represent key Resource component of the Resource Center with
disease, injury, and disability. The CDC Center audiences: Employers (N=10), approximately 5 selected states using
Workplace Health Promotion Resource business groups (N=10), vendors and two online surveys: a TA feedback
Center is authorized by the Public consultants (N=12), public health survey and TA pilot assessment. The TA
Health Service Act and funded through organizations (N=4), journalists (N=4), feedback survey will be offered to up to
the Prevention and Public Health Fund and researchers (N=10). Each tailored 100 stakeholders after each TA
of the Patient Protection and Affordable interview will be 45–60 minutes in encounter and will take approximately
Care Act (ACA). length. Additional information will be 5 minutes. The TA pilot assessment will
Resource Center development and collected through an online Needs and be provided at the conclusion of the TA
information collection will be Interests Market Survey involving 800 pilot to up to 100 stakeholders and will
conducted in two phases over a three- respondents. Findings will be used to take approximately 20 minutes.
year period. In Phase 1 (project years 1 tailor the contents, technical support Findings will be used to improve
and 2), CDC will conduct formative and dissemination practices of the
workplace health programs and the
research to understand the needs and Resource Center to the needs and
preferences of the target audience. In offerings of the Resource Center.
interests of the target audiences.
Phase 2 (project years 2 and 3), CDC will During Phase 2, Resource Center OMB approval is requested for three
build the Resource Center and IC, products will be launched and CDC will years. Participation is voluntary and
provide technical assistance, and assess collect brief, online customer there are no costs to respondents other
customer satisfaction. satisfaction surveys from approximately than their time.
ESTIMATED ANNUALIZED BURDEN HOURS
Average
Number of Total
Number of burden per
Type of respondents Form name responses per burden
respondents response
respondent (in hrs.)
(in hrs.)
Employers ............................................. Needs and Interests Interview Guide 3 1 1 3
for Employers.
Business Groups, Vendors, Consult- Needs and Interests Interview Guide 9 1 1 9
ants, and Public Health Organiza- for Business Groups, Vendors, Con-
tions. sultants, and Public Health Organi-
zations.
Journalists ............................................. Needs and Interests Interview Guide 1 1 45/60 1
for Journalists.
Researchers .......................................... Needs and Interests Interview Guide 3 1 45/60 2
for the Research Community.
Key Stakeholders and Users of the Re- Stakeholder Needs and Interests Mar- 267 1 20/60 89
source Center (All Groups). ket Survey.
Consumer Satisfaction Survey ............. 283 1 2/60 9
Technical Assistance ............................ TA Feedback Survey ........................... 33 5 5/60 14
(TA) Participants ................................... TA Pilot Assessment ............................ 33 1 20/60 11
Total ............................................... ............................................................... ........................ ........................ ........................ 138
Leroy A. Richardson, ACTION: Notice with comment period. • Federal eRulemaking Portal:
Chief, Information Collection Review Office, Regulation.gov. Follow the instructions
Office of Scientific Integrity, Office of the SUMMARY: The Centers for Disease for submitting comments.
Associate Director for Science, Office of the Control and Prevention (CDC), as part of • Mail: Leroy A. Richardson,
Director, Centers for Disease Control and its continuing efforts to reduce public Information Collection Review Office,
Prevention. burden and maximize the utility of
Centers for Disease Control and
[FR Doc. 2016–09638 Filed 4–25–16; 8:45 am] government information, invites the
Prevention, 1600 Clifton Road, NE.,
BILLING CODE 4163–18–P general public and other Federal
MS–D74, Atlanta, Georgia 30329.
agencies to take this opportunity to
Instructions: All submissions received
comment on proposed and/or
continuing information collections, as must include the agency name and
DEPARTMENT OF HEALTH AND
required by the Paperwork Reduction Docket Number. All relevant comments
HUMAN SERVICES
Act of 1995. This notice invites received will be posted without change
Centers for Disease Control and comment on an extension request for to Regulations.gov, including any
Prevention the information collection entitled personal information provided. For
Application for Permit to Import access to the docket to read background
[60Day-16–0199; Docket No. CDC–2016– Biological Agents and Vectors of Human documents or comments received, go to
0039] Disease into the United States and Regulations.gov.
mstockstill on DSK4VPTVN1PROD with NOTICES
Application for Permit to Import or Please note: All public comment should be
Proposed Data Collection Submitted Transport Live Bats (42 CFR 71.54). submitted through the Federal eRulemaking
for Public Comment and portal (Regulations.gov) or by U.S. mail to the
DATES: Written comments must be
Recommendations address listed above.
received on or before June 27, 2016.
AGENCY: Centers for Disease Control and ADDRESSES: You may submit comments, FOR FURTHER INFORMATION CONTACT: To
Prevention (CDC), Department of Health identified by Docket No. CDC–2016– request more information on the
and Human Services (HHS). 0039 by any of the following methods: proposed project or to obtain a copy of
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![24618 Federal Register / Vol. 81, No. 80 / Tuesday, April 26, 2016 / Notices
Leroy A. Richardson, and U.S.C. 9858. The Plan provides ACF 2014 made significant changes to the
Chief, Information Collection Review Office, and the public with a description of, CCDF program. However, the law did
Office of Scientific Integrity, Office of the and assurances about, the Tribes’ child not explicitly indicate the extent to
Associate Director for Science, Office of the care program. which many of the new requirements
Director, Centers for Disease Control and The FY 2017–2019 CCDF Plan apply to Tribes. Questions related to the
Prevention. Preprint for Tribal grantees is being CCDBG Act of 2014 will provide ACF
[FR Doc. 2016–09657 Filed 4–25–16; 8:45 am] published in the Federal Register for a with baseline information on Tribal
BILLING CODE 4163–18–P 30-day Public Comment Period to practices and technical assistance
provide an opportunity for the public to needs.
submit comments to the Office of
DEPARTMENT OF HEALTH AND Management and Budget (OMB). The ACF extended the current Tribal Plan
HUMAN SERVICES first 60-day comment period on the for one year, which means that Tribes
Tribal Preprint closed on March 19, will submit new 3-year Plans for FY
Administration for Children and 2016. The Office of Child Care (OCC) 2017–2019 on July 1, 2016, with an
Families has given thoughtful consideration to effective date of October 1, 2016. This
those comments received during the 60- additional time allowed the Office of
Submission for OMB Review; Child Care to consult with Tribal
Comment Request day Public Comment Period. The Plan
has been revised to provide additional Leaders and their designated
guidance and clarification throughout representatives to solicit input on how
Title: Child Care Development Fund
the document to improve the quality of the new requirements of the CCDBG Act
Plan for Tribes for FFY 2017–2019
the information requested. Additional of 2014 might apply to Tribal child care
(ACF–118–A).
OMB No.: 0970–0198. revisions were also made to identify programs. HHS will publish a Final
Description: The Child Care and those questions related to the CCDBG Rule to determine the extent to which
Development Fund (CCDF) Plan (the Act of 2014 that were added for the new law applies to Tribes. Pending
Plan) for Tribes is required from each ‘‘informational purposes only’’. A red the issuance of new regulations and
CCDF Lead Agency in accordance with delta sign has been inserted to guidance, Tribes are subject to the prior
Section 658E of the Child Care and specifically identify those questions law and regulations.
Development Block Grant (CCDBG) Act, related to the new law. The CCDBG Act Respondents: Tribal CCDF Lead
as amended, by Public Law 113–186 of 2014, signed into law in November of Agencies (257).
ANNUAL BURDEN ESTIMATES
Number of Average
Number of Total burden
Instrument responses per burden hours
respondents hours
respondent per response
ACF–118–A ..................................................................................................... 257 0.50 120 15,420
Estimated Total Annual Burden Desk Officer for the Administration for provide funds to states that will enable
Hours: 15,420. Children and Families. them to provide services for the purpose
Additional Information: Copies of the of increasing noncustodial parent (NCP)
Robert Sargis,
proposed collection may be obtained by access to and visitation with their
Reports Clearance Officer. children. State governors decide which
writing to the Administration for [FR Doc. 2016–09618 Filed 4–25–16; 8:45 am] state entity will be responsible for
Children and Families, Office of BILLING CODE 4184–01–P implementing the AV grant program and
Planning, Research and Evaluation, 330
the state determines who will be served,
C Street SW., Washington, DC 20201. what services will be provided, and
Attention Reports Clearance Officer. All DEPARTMENT OF HEALTH AND whether the services will be statewide
requests should be identified by the title HUMAN SERVICES or in local jurisdictions. The statute
of the information collection. Email specifies certain activities which may be
address: infocollection@acf.hhs.gov. Administration for Children and
Families funded, including: voluntary and
OMB Comment: OMB is required to mandatory mediation, counseling,
make a decision concerning the Submission for OMB Review; education, the development of parenting
collection of information between 30 Comment Request plans, supervised visitation, and the
and 60 days after publication of this development of guidelines for visitation
document in the Federal Register. Title: State Access and Visitation and alternative custody arrangements.
Therefore, a comment is best assured of Grant Application. Even though OCSE manages this
having its full effect if OMB receives it OMB No.: 0970—NEW. program, the funding for the AV grant
within 30 days of publication. Written is separate from funding for federal and
Description state administration of the Child
comments and recommendations for the
Support program.
mstockstill on DSK4VPTVN1PROD with NOTICES
proposed information collection should The Personal Responsibility and Work
be sent directly to the following: Office Opportunity Reconciliation Act of 1996 Section 469B(e)(3) of the Social
of Management and Budget, Paperwork (PRWORA) created the ‘‘Grants to States Security Act (Pub. L. 104–193) requires
Reduction Project, Email: OIRA_ for Access and Visitation’’ program (AV that each state receiving an Access and
SUBMISSION@OMB.EOP.GOV, Attn: grant program). Funding for the program Visitation (AV) grant award monitor,
began in FY 1997 with a capped, annual evaluate and report on such programs in
entitlement of $10 million. The accordance with regulations (45 CFR
statutory goal of the program is to part 303). The AV Grant Program Terms
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Document Created: 2016-04-26 01:36:37
Document Modified: 2016-04-26 01:36:37
| 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 with comment period. | |
| Dates | Written comments must be received on or before June 27, 2016. | |
| Contact | To request more information on the proposed project or to obtain a copy of the information collection plan and instruments, contact the Information Collection Review Office, Centers for Disease Control and Prevention, 1600 Clifton Road, NE., MS-D74, Atlanta, Georgia 30329; phone: 404-639-7570; Email: [email protected] | |
| FR Citation | 81 FR 24616 |
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