Proposed Data Collection Submitted for Public Comment and Recommendations, 60906-60908 [2015-25646]
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60906
Federal Register / Vol. 80, No. 195 / Thursday, October 8, 2015 / Notices
health care, quality of life, social and
educational outcomes, and transition of
care from childhood to adulthood. The
information collected from this
population-based survey will be used to
inform current knowledge, allocate
resources, develop services, and,
ultimately, improve long-term health of
adults born with CHD.
We estimate identifying 7,500
individuals with CHD in the birth
defects surveillance systems, obtaining
current addresses and sending surveys
to 5,625 individuals with CHD (75%),
and receiving completed surveys from
4,500 individuals (80%). The survey
takes approximately 25 minutes to
complete, which includes 5 minutes to
read the informed consent and 20
minutes to answer survey questions.
Therefore, we estimate the total burden
hours are 1,875.
There are no costs to participants
other than their time.
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents
Number of
responses per
respondent
Average
burden per
response
(in hours)
Total burden
hours
Type of respondent
Form name
Individuals with CHD .........................
Individuals with CHD .........................
Informed consent ...........................
Survey ............................................
4,500
4,500
1
1
5/60
20/60
375
1,500
Total ...........................................
.........................................................
........................
..........................
........................
1,875
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. 2015–25647 Filed 10–7–15; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60 Day–16–15BHH; Docket No. CDC–2016–
0087]
Proposed Data Collection Submitted
for Public Comment and
Recommendations
Centers for Disease Control and
Prevention (CDC), Department of Health
and Human Services (HHS).
ACTION: Notice with comment period.
AGENCY:
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 the Personal Protective
Equipment Information (PPE-Info)
Database which is a compendium of
personal protective equipment (PPE)
Federal regulations and consensus
standards.
mstockstill on DSK4VPTVN1PROD with NOTICES
SUMMARY:
Written comments must be
received on December 7, 2015.
DATES:
VerDate Sep<11>2014
16:41 Oct 07, 2015
Jkt 238001
You may submit comments,
identified by Docket No. CDC–2016–
0087 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.
ADDRESSES:
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.
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: omb@cdc.gov.
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
FOR FURTHER INFORMATION CONTACT:
PO 00000
Frm 00035
Fmt 4703
Sfmt 4703
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.
E:\FR\FM\08OCN1.SGM
08OCN1
60907
Federal Register / Vol. 80, No. 195 / Thursday, October 8, 2015 / Notices
Proposed Project
PPE-Info Database—New—National
Institute for Occupational Safety and
Health (NIOSH), Centers for Disease
Control and Prevention (CDC).
Background and Brief Description
The mission of the National Institute
for Occupational Safety and Health
(NIOSH) is to promote safety and health
at work for all people through research
and prevention. Under Public Law 91–
173 as amended by Public Law 95–164
(Federal Mine Safety and Health Act of
1977), NIOSH is proposing a three-year
study to conduct research to advance
the health and safety of workers.
National Personal Protective
Technology Laboratory (NPPTL)
developed the NIOSH PPE-Info Database
in response to recommendations from
the Institute of Medicine (IOM) in its
report, Certifying Personal Protective
Technologies (PPT): Improving Worker
Safety. The report recommended that
NPPTL ‘‘expand its efforts to become a
national clearinghouse for information
on all types of PPT.’’
In its current application, the database
provides standards developers,
manufacturers, purchasers, and end
users of PPE with a comprehensive tool
which allows general or advanced
criteria searches of relevant standards,
target occupational groups, basic
conformity assessment specifications,
accredited lab information, and
standard connections.
The CDC is currently updating its PPE
selection guidance related to the Ebola
response. This guidance, Guidance on
Personal Protective Equipment To Be
Used by Healthcare Workers During
Management of Patients with Ebola
Virus Disease in U.S. Hospitals,
Including Procedures for Putting On
(Donning) and Removing (Doffing)
(hereafter referred to as the ‘‘CDC Ebola
Response PPE Guidance’’) will provide
recommendations, in the form of
protection standards, for PPE selection
and use for the Ebola response.
The NIOSH PPE-Info Database is
being expanded as a tool to connect the
protection standards that already exist
in the database, with relevant PPE
information as identified through the
updated CDC Ebola Response PPE
Guidance. This new aspect of the
NIOSH PPE-Info Database allows end
users (e.g., healthcare workers) to find
products (e.g., gowns and coveralls) that
are compliant (as verified by
manufacturer) with the protection
standards outlined by the CDC Ebola
Response PPE Guidance. The initial
information in the NIOSH PPE-Info
Database will only offer guidance on
gowns and coveralls, but is intended to
expand to all PPE types associated with
the official CDC Ebola Response PPE
Guidance in the future. Since there is no
single source of this information,
NOISH is requesting that Manufactures
provide it directly for input into the
Ebola PPE selection guidance portion of
the database.
NIOSH is requesting that a
Memorandum of Understanding (MOU)
be developed with Ebola response PPE
manufacturers to facilitate cooperation
and collaboration on the provision of
product information. The primary focus
of the collaboration will be the exchange
of manufacturer product information to
be aggregated and displayed in the
NIOSH PPE-Info Database.
The nature and use of this
information exchange includes the (1)
provision of product information
regarding compliance (as verified by
manufacturers) with designated
protection standards related to CDC
guidance for personal protective
equipment (PPE) used by healthcare
workers during management of patients
with confirmed or suspected Ebola
Virus Disease (‘‘Ebola’’) and (2) the
verification, by manufacturers, of
product information displayed in the
NIOSH PPE-Info Database.
Once the MOU is signed, the
manufacturer will be sent a product
information sheet. Using he product
information sheet, NIOSH collects
manufacturer-specific product
information such as; product category
(e.g., gown or coverall), standards that
the product claim complies with,
product model number, product name,
link to product specification sheet from
manufacturer, and designation of
whether third-party testing was
performed. Once this information is
completed, the product information
sheet is electronically signed and
returned by email to NIOSH. The
NIOSH project officer will then upload
the information into a PPE-Info sub
database, which acts as an interim point
for review. The manufacturer is then
sent a link to the sub database to review
their products. The manufacturer has
one week to make objections. If no
objections are made, the information in
the sub-database gets published to the
live NIOSH PPE-Info database.
Quarterly, manufacturer products will
be pulled from the database and sent
through a pre generated product
information sheet to the manufacturer
POC. Manufacturers are required
through the MOU to complete and
return the PPE Information Sheet within
two weeks of receipt along with the
electronic verification form.
NIOSH will be soliciting information
from manufacturers and manufacturer
POCs. For products that comply with
gown and coverall standards, we
estimate that seven manufacturers will
need to supply product information.
The amount of time for manufacturers to
complete the initial product information
sheets and make quarterly updated will
be no more than 3 hours for the initial
product information and one hour for
the quarterly updates. The total
estimated burden hours are 42. There
are no costs to respondents other than
their time.
ESTIMATED ANNUALIZED BURDEN HOURS
Number
responses per
respondent
Number of
respondents
Average
burden per
response
(in hours)
Total
burden
hours
Form name
Manufacturer .............................................
Manufacturer POC ....................................
mstockstill on DSK4VPTVN1PROD with NOTICES
Type of respondent
Initial Product Info Sheet ..............
Quarterly product Info Sheet ........
7
7
1
3
3
1
21
Total ...................................................
.......................................................
........................
..........................
........................
42
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Fmt 4703
Sfmt 4703
E:\FR\FM\08OCN1.SGM
08OCN1
60908
Federal Register / Vol. 80, No. 195 / Thursday, October 8, 2015 / Notices
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. 2015–25646 Filed 10–7–15; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
[60Day–16–0234; Docket No. CDC–2015–
0086]
Proposed Data Collection Submitted
for Public Comment and
Recommendations
Centers for Disease Control and
Prevention (CDC), Department of Health
and Human Services (HHS).
ACTION: Notice with comment period.
AGENCY:
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 the proposed revision of
the National Ambulatory Medical Care
Survey (NAMCS). The purpose of
NAMCS is to meet the needs and
demands for statistical information
about the provision of ambulatory
medical care services in the United
States.
SUMMARY:
Written comments must be
received on or before December 7, 2015.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2016–
0026 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.
mstockstill on DSK4VPTVN1PROD with NOTICES
VerDate Sep<11>2014
16:41 Oct 07, 2015
Jkt 238001
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.
SUPPLEMENTARY INFORMATION:
Centers for Disease Control and
Prevention
DATES:
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: omb@cdc.gov.
FOR FURTHER INFORMATION CONTACT:
PO 00000
Frm 00037
Fmt 4703
Sfmt 4703
Proposed Project
The National Ambulatory Medical
Care Survey (NAMCS), (OMB No. 0920–
0234, expires 12/31/2017)—Revision —
National Center for Health Statistics
(NCHS), Centers for Disease Control and
Prevention (CDC).
Background and Brief Description
Section 306 of the Public Health
Service (PHS) Act (42 U.S.C. 242k), as
amended, authorizes that the Secretary
of Health and Human Services, acting
through NCHS, shall collect statistics on
the utilization of health care provided
by non-federal office-based physicians
in the United States. On December 19,
2014, the OMB approved data collection
for three years from 2015 to 2017. This
revision is to request approval to
continue NAMCS data collection
activities for three years from 2016–
2018 and to add questions to the
physician interview that pertain to
policies, services, and experiences
related to the prevention and treatment
of sexually transmitted infections (STIs)
and HIV prevention among adolescents
and others. Small modifications will
also be made to questions on the use of
electronic health records. This notice
also covers a decrease in the sample size
resulting from smaller budget
allocations. Due to this decrease,
selected state estimates will not be
available for 2016–2018 data.
The National Ambulatory Medical
Care Survey (NAMCS) has been
conducted intermittently from 1973
through 1985, and annually since 1989.
The purpose of NAMCS, a voluntary
survey, is to meet the needs and
demands for statistical information
about the provision of ambulatory
medical care services in the United
States. Ambulatory services are
rendered in a wide variety of settings,
including physicians’ offices and
hospital outpatient and emergency
departments.
The NAMCS target universe consists
of all office visits made by ambulatory
patients to non-Federal office-based
physicians (excluding those in the
specialties of anesthesiology, radiology,
and pathology) who are engaged in
direct patient care. In 2006, physicians
and mid-level providers (i.e., nurse
practitioners, physician assistants, and
nurse midwives) practicing in
community health centers (CHCs) were
added to the NAMCS sample, and these
data will continue to be collected.
To complement NAMCS data, NCHS
initiated the National Hospital
Ambulatory Medical Care Survey
(NHAMCS, OMB No. 0920–0278,
expires 02/28/18) in 1992 to provide
E:\FR\FM\08OCN1.SGM
08OCN1
]]>Agencies
[Federal Register Volume 80, Number 195 (Thursday, October 8, 2015)]
[Notices]
[Pages 60906-60908]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2015-25646]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[60 Day-16-15BHH; Docket No. CDC-2016-0087]
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 the Personal
Protective Equipment Information (PPE-Info) Database which is a
compendium of personal protective equipment (PPE) Federal regulations
and consensus standards.
DATES: Written comments must be received on December 7, 2015.
ADDRESSES: You may submit comments, identified by Docket No. CDC-2016-
0087 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 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: omb@cdc.gov.
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.
[[Page 60907]]
Proposed Project
PPE-Info Database--New--National Institute for Occupational Safety
and Health (NIOSH), Centers for Disease Control and Prevention (CDC).
Background and Brief Description
The mission of the National Institute for Occupational Safety and
Health (NIOSH) is to promote safety and health at work for all people
through research and prevention. Under Public Law 91-173 as amended by
Public Law 95-164 (Federal Mine Safety and Health Act of 1977), NIOSH
is proposing a three-year study to conduct research to advance the
health and safety of workers.
National Personal Protective Technology Laboratory (NPPTL)
developed the NIOSH PPE-Info Database in response to recommendations
from the Institute of Medicine (IOM) in its report, Certifying Personal
Protective Technologies (PPT): Improving Worker Safety. The report
recommended that NPPTL ``expand its efforts to become a national
clearinghouse for information on all types of PPT.''
In its current application, the database provides standards
developers, manufacturers, purchasers, and end users of PPE with a
comprehensive tool which allows general or advanced criteria searches
of relevant standards, target occupational groups, basic conformity
assessment specifications, accredited lab information, and standard
connections.
The CDC is currently updating its PPE selection guidance related to
the Ebola response. This guidance, Guidance on Personal Protective
Equipment To Be Used by Healthcare Workers During Management of
Patients with Ebola Virus Disease in U.S. Hospitals, Including
Procedures for Putting On (Donning) and Removing (Doffing) (hereafter
referred to as the ``CDC Ebola Response PPE Guidance'') will provide
recommendations, in the form of protection standards, for PPE selection
and use for the Ebola response.
The NIOSH PPE-Info Database is being expanded as a tool to connect
the protection standards that already exist in the database, with
relevant PPE information as identified through the updated CDC Ebola
Response PPE Guidance. This new aspect of the NIOSH PPE-Info Database
allows end users (e.g., healthcare workers) to find products (e.g.,
gowns and coveralls) that are compliant (as verified by manufacturer)
with the protection standards outlined by the CDC Ebola Response PPE
Guidance. The initial information in the NIOSH PPE-Info Database will
only offer guidance on gowns and coveralls, but is intended to expand
to all PPE types associated with the official CDC Ebola Response PPE
Guidance in the future. Since there is no single source of this
information, NOISH is requesting that Manufactures provide it directly
for input into the Ebola PPE selection guidance portion of the
database.
NIOSH is requesting that a Memorandum of Understanding (MOU) be
developed with Ebola response PPE manufacturers to facilitate
cooperation and collaboration on the provision of product information.
The primary focus of the collaboration will be the exchange of
manufacturer product information to be aggregated and displayed in the
NIOSH PPE-Info Database.
The nature and use of this information exchange includes the (1)
provision of product information regarding compliance (as verified by
manufacturers) with designated protection standards related to CDC
guidance for personal protective equipment (PPE) used by healthcare
workers during management of patients with confirmed or suspected Ebola
Virus Disease (``Ebola'') and (2) the verification, by manufacturers,
of product information displayed in the NIOSH PPE-Info Database.
Once the MOU is signed, the manufacturer will be sent a product
information sheet. Using he product information sheet, NIOSH collects
manufacturer-specific product information such as; product category
(e.g., gown or coverall), standards that the product claim complies
with, product model number, product name, link to product specification
sheet from manufacturer, and designation of whether third-party testing
was performed. Once this information is completed, the product
information sheet is electronically signed and returned by email to
NIOSH. The NIOSH project officer will then upload the information into
a PPE-Info sub database, which acts as an interim point for review. The
manufacturer is then sent a link to the sub database to review their
products. The manufacturer has one week to make objections. If no
objections are made, the information in the sub-database gets published
to the live NIOSH PPE-Info database.
Quarterly, manufacturer products will be pulled from the database
and sent through a pre generated product information sheet to the
manufacturer POC. Manufacturers are required through the MOU to
complete and return the PPE Information Sheet within two weeks of
receipt along with the electronic verification form.
NIOSH will be soliciting information from manufacturers and
manufacturer POCs. For products that comply with gown and coverall
standards, we estimate that seven manufacturers will need to supply
product information. The amount of time for manufacturers to complete
the initial product information sheets and make quarterly updated will
be no more than 3 hours for the initial product information and one
hour for the quarterly updates. The total estimated burden hours are
42. There are no costs to respondents other than 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
----------------------------------------------------------------------------------------------------------------
Manufacturer................... Initial Product 7 1 3
Info Sheet.
Manufacturer POC............... Quarterly product 7 3 1 21
Info Sheet.
------------------------------------------------------------
Total...................... .................. .............. ............... .............. 42
----------------------------------------------------------------------------------------------------------------
[[Page 60908]]
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. 2015-25646 Filed 10-7-15; 8:45 am]
BILLING CODE 4163-18-P
