81 FR 54580 - 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 158 (August 16, 2016)
Centers for Disease Control and Prevention
Federal Register Volume 81, Issue 158 (August 16, 2016)
| Page Range | 54580-54581 | |
| FR Document | 2016-19461 |
[Federal Register Volume 81, Number 158 (Tuesday, August 16, 2016)] [Notices] [Pages 54580-54581] From the Federal Register Online [www.thefederalregister.org] [FR Doc No: 2016-19461] ----------------------------------------------------------------------- DEPARTMENT OF HEALTH AND HUMAN SERVICES Centers for Disease Control and Prevention [Docket No. CDC-2016-0083; 60Day-16-16AWM] Proposed Data Collection Submitted for Public Comment and Recommendations AGENCY: Centers for Disease Control and Prevention, Department of Health and Human Services. ACTION: Notice with comment period. ----------------------------------------------------------------------- SUMMARY: Centers for Disease Control and Prevention 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 this proposed information collections, as required by the Paperwork Reduction Act of 1995. This notice invites comment on the Executive and Scientific Resources Office Access Management System (EAMTS). EAMTS is designed to house all Guest Researcher & ORISE program packets, Appointment Mechanism Determination Forms, and Title 42 Fellowship Immigration information in one central location on the Human Resources Office SharePoint Server. DATES: Written comments must be received on or before October 17, 2016. ADDRESSES: You may submit comments, identified by Docket No. CDC-2016- 0083 by any of the following methods: Federal eRulemaking Portal: Regulations.gov. Follow the instructions for submitting comments. Mail: Jeffrey M. Zirger, Acting 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. 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 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 Data Management for Executive and Scientific Resources Access Management Tracking System--New--Executive and Scientific Resource Office (ESRO), Centers for Disease Control and Prevention (CDC). Background and Brief Description ESRO seeks to submit and information collection request for approval of information collections through its ESRO Access Management Tracking System (EAMTS). This system will automate current manual processes for programs managed by ESRO. This new process will provide users a single, integrated location to allow for collaboration, faster processing between the programs and ESRO and a better onboarding experience for potential fellows. EAMTS will support users by providing a single, integrated location for enterprise content management, manage documents and records by using workflows an information rights management. This business process will allow ESRO to design forms that are accessible in SharePoint through a Web Browser. Team members will be able to access critical business information, analyze and view data, and publish reports to make more informed decisions. EAMTS will allow CIO's to submit digital packets including Guest Researcher, ORISE, Title 42 Fellowship Visa request (portion of CDC 0.1475) and Appointment Mechanism Determination Request Form (CDC 0.4601). CIO's can upload supplemental documentation as an attachment to each application, electronically track and monitor status of application, digitally sign forms and requests, receive case determinations quickly and accurately, and track the Visa status of Title 42 Fellowship requests that require Visa assistance from the Human Resources Office. EAMTS is developed in SharePoint for CDC's Centers/Institutes/ Offices (CIO) to submit required information for all of Executive and Scientific Resource Office's managed programs and for these CIO's to effectively and efficiently digitally review this information. Data is managed and maintained by appropriate CIO Staff with ground and form level permission. Permissions to EAMTS are required to access the lists, forms, and document library. This includes entering data, [[Page 54581]] clearing/approving forms, processing forms, and acknowledging data entered. The total estimated annualized burden hours for all respondents are 1,280. There are no costs to respondents other than their time. CDC will seek a three-year approval from OMB. Estimated Annualized Burden Hours ---------------------------------------------------------------------------------------------------------------- Number of Average burden Type of respondents Form name Number of responses per per response Total burden respondents CIO (in hours) (in hours) ---------------------------------------------------------------------------------------------------------------- Initiator/C/I/O............... CDC 0.4601...... 64 5 1 320 Initiator/C/I/O............... CDC 0.410A...... 64 5 1 320 Initiator/C/I/O............... CDC 0.410B...... 64 5 1 320 Initiator/C/I/O............... Section C of the 64 5 1 320 CDC 0.1475. --------------------------------------------------------------- Totals.................... ................ .............. .............. .............. 1,280 ---------------------------------------------------------------------------------------------------------------- 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. 2016-19461 Filed 8-15-16; 8:45 am] BILLING CODE 4163-18-P
![54580 Federal Register / Vol. 81, No. 158 / Tuesday, August 16, 2016 / Notices
Leroy A. Richardson, Note: All public comment should be the collection of information; and to
Chief, Information Collection Review Office, submitted through the Federal eRulemaking transmit or otherwise disclose the
Office of Scientific Integrity, Office of the portal (Regulations.gov) or by U.S. mail to the information.
Associate Director for Science, Office of the address listed above.
Director, Centers for Disease Control and Proposed Project
FOR FURTHER INFORMATION CONTACT: To
Prevention. Data Management for Executive and
request more information on the
[FR Doc. 2016–19460 Filed 8–15–16; 8:45 am] Scientific Resources Access
proposed project or to obtain a copy of
BILLING CODE 4163–18–P
the information collection plan and Management Tracking System—New—
instruments, contact the Information Executive and Scientific Resource Office
Collection Review Office, Centers for (ESRO), Centers for Disease Control and
DEPARTMENT OF HEALTH AND Prevention (CDC).
Disease Control and Prevention, 1600
HUMAN SERVICES
Clifton Road NE., MS–D74, Atlanta, Background and Brief Description
Centers for Disease Control and Georgia 30329; phone: 404–639–7570;
Email: omb@cdc.gov. ESRO seeks to submit and
Prevention
SUPPLEMENTARY INFORMATION: Under the information collection request for
[Docket No. CDC–2016–0083; 60Day–16– Paperwork Reduction Act of 1995 (PRA) approval of information collections
16AWM] through its ESRO Access Management
(44 U.S.C. 3501–3520), Federal agencies
must obtain approval from the Office of Tracking System (EAMTS). This system
Proposed Data Collection Submitted will automate current manual processes
for Public Comment and Management and Budget (OMB) for each
collection of information they conduct for programs managed by ESRO. This
Recommendations new process will provide users a single,
or sponsor. In addition, the PRA also
AGENCY: Centers for Disease Control and requires Federal agencies to provide a integrated location to allow for
Prevention, Department of Health and 60-day notice in the Federal Register collaboration, faster processing between
Human Services. concerning each proposed collection of the programs and ESRO and a better
ACTION: Notice with comment period. information, including each new onboarding experience for potential
proposed collection, each proposed fellows.
SUMMARY: Centers for Disease Control extension of existing collection of EAMTS will support users by
and Prevention as part of its continuing information, and each reinstatement of providing a single, integrated location
efforts to reduce public burden and previously approved information for enterprise content management,
maximize the utility of government collection before submitting the manage documents and records by using
information, invites the general public collection to OMB for approval. To workflows an information rights
and other Federal agencies to take this comply with this requirement, we are management. This business process will
opportunity to comment on this publishing this notice of a proposed allow ESRO to design forms that are
proposed information collections, as data collection as described below. accessible in SharePoint through a Web
required by the Paperwork Reduction Comments are invited on: (a) Whether Browser. Team members will be able to
Act of 1995. This notice invites the proposed collection of information access critical business information,
comment on the Executive and is necessary for the proper performance analyze and view data, and publish
Scientific Resources Office Access of the functions of the agency, including reports to make more informed
Management System (EAMTS). EAMTS whether the information shall have decisions.
is designed to house all Guest practical utility; (b) the accuracy of the EAMTS will allow CIO’s to submit
Researcher & ORISE program packets, agency’s estimate of the burden of the digital packets including Guest
Appointment Mechanism Determination proposed collection of information; (c) Researcher, ORISE, Title 42 Fellowship
Forms, and Title 42 Fellowship ways to enhance the quality, utility, and Visa request (portion of CDC 0.1475)
Immigration information in one central clarity of the information to be and Appointment Mechanism
location on the Human Resources Office collected; (d) ways to minimize the Determination Request Form (CDC
SharePoint Server. burden of the collection of information 0.4601). CIO’s can upload supplemental
DATES: Written comments must be on respondents, including through the documentation as an attachment to each
received on or before October 17, 2016. use of automated collection techniques application, electronically track and
ADDRESSES: You may submit comments, or other forms of information monitor status of application, digitally
identified by Docket No. CDC–2016– technology; and (e) estimates of capital sign forms and requests, receive case
0083 by any of the following methods: or start-up costs and costs of operation, determinations quickly and accurately,
Federal eRulemaking Portal: maintenance, and purchase of services and track the Visa status of Title 42
Regulations.gov. Follow the instructions to provide information. Burden means Fellowship requests that require Visa
for submitting comments. the total time, effort, or financial assistance from the Human Resources
Mail: Jeffrey M. Zirger, Acting resources expended by persons to Office.
Information Collection Review Office, generate, maintain, retain, disclose or EAMTS is developed in SharePoint
Centers for Disease Control and provide information to or for a Federal for CDC’s Centers/Institutes/Offices
Prevention, 1600 Clifton Road NE., MS– agency. This includes the time needed (CIO) to submit required information for
D74, Atlanta, Georgia 30329. to review instructions; to develop, all of Executive and Scientific Resource
Instructions: All submissions received acquire, install and utilize technology Office’s managed programs and for these
asabaliauskas on DSK3SPTVN1PROD with NOTICES
must include the agency name and and systems for the purpose of CIO’s to effectively and efficiently
Docket Number. All relevant comments collecting, validating and verifying digitally review this information. Data is
received will be posted without change information, processing and managed and maintained by appropriate
to Regulations.gov, including any maintaining information, and disclosing CIO Staff with ground and form level
personal information provided. For and providing information; to train permission.
access to the docket to read background personnel and to be able to respond to Permissions to EAMTS are required to
documents or comments received, go to a collection of information, to search access the lists, forms, and document
Regulations.gov. data sources, to complete and review library. This includes entering data,
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![Federal Register / Vol. 81, No. 158 / Tuesday, August 16, 2016 / Notices 54581
clearing/approving forms, processing The total estimated annualized other than their time. CDC will seek a
forms, and acknowledging data entered. burden hours for all respondents are three-year approval from OMB.
1,280. There are no costs to respondents
ESTIMATED ANNUALIZED BURDEN HOURS
Average
Number of
Number of burden per Total burden
Type of respondents Form name responses per
respondents response (in hours)
CIO (in hours)
Initiator/C/I/O ..................................... CDC 0.4601 ..................................... 64 5 1 320
Initiator/C/I/O ..................................... CDC 0.410A ..................................... 64 5 1 320
Initiator/C/I/O ..................................... CDC 0.410B ..................................... 64 5 1 320
Initiator/C/I/O ..................................... Section C of the CDC 0.1475 .......... 64 5 1 320
Totals ......................................... ........................................................... ........................ ........................ ........................ 1,280
Leroy A. Richardson, Bethesda, MD 20892–9823, (240) 669–5069, Reference No. E–157–2011/0–US–01],
Chief, Information Collection Review Office, lrust@niaid.nih.gov. status: Expired;
Office of Scientific Integrity, Office of the (Catalogue of Federal Domestic Assistance International Patent Application No.
Associate Director for Science, Office of the Program Nos. 93.855, Allergy, Immunology, PCT/US2012/32772 filed April 9, 2012
Director, Centers for Disease Control and and Transplantation Research; 93.856, titled ‘‘Small molecule therapeutic
Prevention. Microbiology and Infectious Diseases
Research, National Institutes of Health, HHS)
compounds targeting thioesterase
[FR Doc. 2016–19461 Filed 8–15–16; 8:45 am]
deficiency disorders and methods of
BILLING CODE 4163–18–P Dated: August 10, 2016. using the same’’ [HHS Reference No. E–
Natasha M. Copeland, 157–2011/0–PCT–02], status: Converted;
Program Analyst, Office of Federal Advisory European Patent Application No.
DEPARTMENT OF HEALTH AND Committee Policy. 12716889.6, filed November 7, 2013,
HUMAN SERVICES [FR Doc. 2016–19417 Filed 8–15–16; 8:45 am] titled ‘‘Small molecule therapeutic
National Institutes of Health BILLING CODE 4140–01–P compounds targeting thioesterase
deficiency disorders and methods of
National Institute of Allergy and using the same’’ [HHS Reference No. E–
Infectious Diseases; Notice of Closed DEPARTMENT OF HEALTH AND 157–2011/0–EP–03], status: Pending;
Meeting HUMAN SERVICES and
United States Patent Application No.
Pursuant to section 10(d) of the National Institutes of Health
14/110,393, filed October 7, 2013, titled
Federal Advisory Committee Act, as ‘‘Small molecule therapeutic
amended (5 U.S.C. App.), notice is Prospective Grant of Start-Up
Exclusive Evaluation Option License compounds targeting thioesterase
hereby given of the following meeting. deficiency disorders and methods of
The meeting will be closed to the Agreement: Small Molecule
Therapeutic Compounds using the same’’ [HHS Reference No. E–
public in accordance with the 157–2011/0–US–04], status: Pending.
provisions set forth in sections Encompassed Within the Licensed
Patent Rights for the Treatment of The patent rights in these inventions
552b(c)(4) and 552b(c)(6), Title 5 U.S.C., have been assigned and/or exclusively
as amended. The grant applications and Thioesterase Deficiency Disorder
licensed to the government of the
the discussions could disclose AGENCY: National Institutes of Health, United States of America.
confidential trade secrets or commercial HHS. The territory of the prospective Start-
property such as patentable material, Up Exclusive Evaluation Option License
and personal information concerning ACTION: Notice.
Agreement may be worldwide and the
individuals associated with the grant field of use may be limited to: ‘‘Small
applications, the disclosure of which SUMMARY: This notice, in accordance
with 35 U.S.C. 209 and 37 CFR part 404, molecule therapeutic compounds
would constitute a clearly unwarranted encompassed within the Licensed
invasion of personal privacy. that the National Institutes of Health,
Department of Health and Human Patent Rights for the treatment of
Name of Committee: National Institute of Services, is contemplating the grant of a thioesterase deficiency disorders’’
Allergy and Infectious Diseases Special Upon the expiration or termination of
Start-Up Exclusive Evaluation Option
Emphasis Panel; NIAID Clinical Trial the Start-up Exclusive Evaluation
Implementation Cooperative Agreement License Agreement to practice the
inventions embodied in the following Option License Agreement, Circumvent
(U01).
Date: September 22, 2016. Patent Applications to Circumvent will have the exclusive right to execute
Time: 10:00 a.m. to 12:00 p.m. Pharmaceuticals Inc. (‘‘Circumvent’’) a Start-Up Exclusive Patent License
Agenda: To review and evaluate grant located in Pasadena, California, USA: Agreement which will supersede and
asabaliauskas on DSK3SPTVN1PROD with NOTICES
applications. replace the Start-up Exclusive
Place: National Institutes of Health, Room Intellectual Property Evaluation Option License Agreement,
3F100, 5601 Fishers Lane, Rockville, MD United States Provisional Patent with no greater field of use and territory
20892 (Telephone Conference Call). than granted in the Start-up Exclusive
Contact Person: Lynn Rust, Ph.D.,
Application No. 61/473,692, filed April
8, 2011, titled ‘‘Small molecule Evaluation Option License Agreement.
Scientific Review Officer, Scientific Review
Program, Division of Extramural Activities, therapeutic compounds targeting DATES: Only written comments and/or
Room 3G42A, National Institutes of Health/ thioesterase deficiency disorders and applications for a license which are
NIAID, 5601 Fishers Lane, MSC 9823, methods of using the same’’ [HHS received by the NIH Office of
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Document Created: 2016-08-16 03:20:41
Document Modified: 2016-08-16 03:20:41
| 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 October 17, 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 54580 |
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