Agency Forms Undergoing Paperwork Reduction Act Review, 9699 [2013-02988]
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9699
Federal Register / Vol. 78, No. 28 / Monday, February 11, 2013 / Notices
Dated: February 5, 2013.
Ron A. Otten,
Director, Office of Scientific Integrity (OSI),
Office of the Associate Director for Science
(OADS), Office of the Director, Centers for
Disease Control and Prevention.
Background and Brief Description
[FR Doc. 2013–02984 Filed 2–8–13; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30Day–13–12PZ]
Agency Forms Undergoing Paperwork
Reduction Act Review
The Centers for Disease Control and
Prevention (CDC) publishes a list of
information collection requests under
review by the Office of Management and
Budget (OMB) in compliance with the
Paperwork Reduction Act (44 U.S.C.
Chapter 35). To request a copy of these
requests, call (404) 639–7570 or send an
email to omb@cdc.gov. Send written
comments to CDC Desk Officer, Office of
Management and Budget, Washington,
DC 20503 or by fax to (202) 395–5806.
Written comments should be received
within 30 days of this notice.
Proposed Project
Proficiency Testing in US Clinical
Laboratories: Perception, Practices and
Potential for Expanded Utility—NEW—
The Office of Surveillance,
Epidemiology and Laboratory Services
(OSELS), Centers for Disease Control
and Prevention (CDC).
The primary focus of this project is to
conduct a systematic analysis in order
to understand which types of
laboratories follow Proficiency Testing
(PT) and Good Laboratory Practices
(GLPs), to identify ways that PT and
GLPs could be better promoted, and to
identify populations that would benefit
from receiving information on PT GLPs.
The Association of Public Health
Laboratories (APHL) and Centers for
Disease Control and Prevention (CDC)
hope to learn more about the perceived
benefits and burden of performing PT.
This information may be helpful to the
CDC as the Clinical Laboratory
Improvement Amendments (CLIA)
regulations for PT are revised. Our
survey population frame is 20,500
Certificate of Compliance laboratories
and 16,800 Certificate of Accreditation
laboratories. All of these laboratories are
required to perform PT in accordance
with CLIA. Many of these laboratories
also use their PT results internally to
further improve laboratory quality at no
additional cost.
The first phase of this project was
conducted by the APHL through focus
group research in 2011. The research
explored how clinical and public health
laboratories perceived commercial PT
programs and explored the ways in
which the laboratories used PT to assure
and improve the quality of their testing.
This second phase of the project will be
administration of a survey to build on
the preliminary findings from the focus
group research and help identify the
types of laboratories that would benefit
from learning about additional uses for
PT. This information will be helpful to
disseminate PT and GLPs to laboratories
in a strategic and targeted way based on
findings from this survey.
The goal is to achieve an 80%
response rate (29,840 out of 37,300
laboratories). APHL and CDC will strive
to ensure a high response rate by
promoting the survey through
advertisements in laboratory trade
publications, at professional meetings,
and possibly through programs and
laboratory accreditation organizations.
The cohort of laboratories surveyed
will be all Certificate of Compliance and
Certificate of Accreditation laboratories
listed in the Centers for Medicare and
Medicaid Services (CMS) Online
Survey, Certification and Reporting
(OSCAR) database. The OSCAR
database contains demographic
information and relevant characteristics
including laboratory specialty and
laboratory type for each laboratory.
The survey will be administered
through a web-based survey system,
specifically Survey Monkey. APHL will
send each laboratory a postmarked letter
explaining the survey and provide them
with a link to log in to the survey with
a unique identifier on their address
label. Two weeks afterwards, APHL will
follow-up with a postcard reminder
which will also include that unique
identifier.
There are no costs to respondents
other than their time.
The annualized estimated burden is
9,947 hours.
Estimated Annualized Burden Hours:
Type of respondent
Form name
Number of
respondents
Number of
responses
per
respondent
Average
burden per
response
(in hrs)
Laboratorians ..................................................
Laboratory Practices ......................................
29,840
1
20/60
Dated: February 5, 2013.
Ron A. Otten,
Director, Office of Scientific Integrity (OSI),
Office of the Associate Director for Science
(OADS), Office of the Director, Centers for
Disease Control and Prevention.
[FR Doc. 2013–02988 Filed 2–8–13; 8:45 am]
Centers for Disease Control and
Prevention
[30Day–13–12PE]
The Centers for Disease Control and
Prevention (CDC) publishes a list of
information collection requests under
review by the Office of Management and
Budget (OMB) in compliance with the
Paperwork Reduction Act (44 U.S.C.
Chapter 35). To request a copy of these
requests, call (404) 639–7570 or send an
VerDate Mar<15>2010
14:26 Feb 08, 2013
Jkt 229001
email to omb@cdc.gov. Send written
comments to CDC Desk Officer, Office of
Management and Budget, Washington,
DC or by fax to (202) 395–5806. Written
comments should be received within 30
days of this notice.
Proposed Project
Agency Forms Undergoing Paperwork
Reduction Act Review
BILLING CODE 4163–18–P
erowe on DSK2VPTVN1PROD with NOTICES
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
PO 00000
Frm 00034
Fmt 4703
Sfmt 4703
Interventions to Reduce Shoulder
MSDs in Overhead Assembly—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
E:\FR\FM\11FEN1.SGM
11FEN1
Agencies
[Federal Register Volume 78, Number 28 (Monday, February 11, 2013)]
[Notices]
[Page 9699]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2013-02988]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[30Day-13-12PZ]
Agency Forms Undergoing Paperwork Reduction Act Review
The Centers for Disease Control and Prevention (CDC) publishes a
list of information collection requests under review by the Office of
Management and Budget (OMB) in compliance with the Paperwork Reduction
Act (44 U.S.C. Chapter 35). To request a copy of these requests, call
(404) 639-7570 or send an email to omb@cdc.gov. Send written comments
to CDC Desk Officer, Office of Management and Budget, Washington, DC
20503 or by fax to (202) 395-5806. Written comments should be received
within 30 days of this notice.
Proposed Project
Proficiency Testing in US Clinical Laboratories: Perception,
Practices and Potential for Expanded Utility--NEW--The Office of
Surveillance, Epidemiology and Laboratory Services (OSELS), Centers for
Disease Control and Prevention (CDC).
Background and Brief Description
The primary focus of this project is to conduct a systematic
analysis in order to understand which types of laboratories follow
Proficiency Testing (PT) and Good Laboratory Practices (GLPs), to
identify ways that PT and GLPs could be better promoted, and to
identify populations that would benefit from receiving information on
PT GLPs. The Association of Public Health Laboratories (APHL) and
Centers for Disease Control and Prevention (CDC) hope to learn more
about the perceived benefits and burden of performing PT. This
information may be helpful to the CDC as the Clinical Laboratory
Improvement Amendments (CLIA) regulations for PT are revised. Our
survey population frame is 20,500 Certificate of Compliance
laboratories and 16,800 Certificate of Accreditation laboratories. All
of these laboratories are required to perform PT in accordance with
CLIA. Many of these laboratories also use their PT results internally
to further improve laboratory quality at no additional cost.
The first phase of this project was conducted by the APHL through
focus group research in 2011. The research explored how clinical and
public health laboratories perceived commercial PT programs and
explored the ways in which the laboratories used PT to assure and
improve the quality of their testing. This second phase of the project
will be administration of a survey to build on the preliminary findings
from the focus group research and help identify the types of
laboratories that would benefit from learning about additional uses for
PT. This information will be helpful to disseminate PT and GLPs to
laboratories in a strategic and targeted way based on findings from
this survey.
The goal is to achieve an 80% response rate (29,840 out of 37,300
laboratories). APHL and CDC will strive to ensure a high response rate
by promoting the survey through advertisements in laboratory trade
publications, at professional meetings, and possibly through programs
and laboratory accreditation organizations.
The cohort of laboratories surveyed will be all Certificate of
Compliance and Certificate of Accreditation laboratories listed in the
Centers for Medicare and Medicaid Services (CMS) Online Survey,
Certification and Reporting (OSCAR) database. The OSCAR database
contains demographic information and relevant characteristics including
laboratory specialty and laboratory type for each laboratory.
The survey will be administered through a web-based survey system,
specifically Survey Monkey. APHL will send each laboratory a postmarked
letter explaining the survey and provide them with a link to log in to
the survey with a unique identifier on their address label. Two weeks
afterwards, APHL will follow-up with a postcard reminder which will
also include that unique identifier.
There are no costs to respondents other than their time.
The annualized estimated burden is 9,947 hours.
Estimated Annualized Burden Hours:
----------------------------------------------------------------------------------------------------------------
Number of Average burden
Type of respondent Form name Number of responses per per response
respondents respondent (in hrs)
----------------------------------------------------------------------------------------------------------------
Laboratorians....................... Laboratory Practices... 29,840 1 20/60
----------------------------------------------------------------------------------------------------------------
Dated: February 5, 2013.
Ron A. Otten,
Director, Office of Scientific Integrity (OSI), Office of the Associate
Director for Science (OADS), Office of the Director, Centers for
Disease Control and Prevention.
[FR Doc. 2013-02988 Filed 2-8-13; 8:45 am]
BILLING CODE 4163-18-P