Proposed Data Collections Submitted for Public Comment and Recommendations, 1790 [2010-510]
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Federal Register / Vol. 75, No. 8 / Wednesday, January 13, 2010 / Notices
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–10–0217]
Proposed Data Collections Submitted
for Public Comment and
Recommendations
In compliance with the requirement
of Section 3506(c)(2)(A) of the
Paperwork Reduction Act of 1995 for
opportunity for public comment on
proposed data collection projects, the
Centers for Disease Control and
Prevention (CDC) will publish periodic
summaries of proposed projects. To
request more information on the
proposed projects or to obtain a copy of
the data collection plans and
instruments, call 404–639–5960 and
send comments to Maryam I. Daneshvar,
CDC Acting Reports Clearance Officer,
1600 Clifton Road, MS–D74, Atlanta,
GA 30333 or send an e-mail to
omb@cdc.gov.
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
States and the Federal government. This
data collection, authorized by 42 U.S.C.
242k, has been carried out by NCHS
since it was created in 1960.
NCHS assists in achieving the
comparability needed for combining
data from all States into national
statistics, by conducting a training
program for State and local vital
statistics staff to assist in developing
expertise in all aspects of vital
registration and vital statistics. The
training offered under this program
includes courses for registration staff,
statisticians, and coding specialists, all
designed to bring about a high degree of
uniformity and quality in the data
provided by the States. This training
program is authorized by 42 U.S.C.
242b, section 304(a). In order to offer the
types of training that would be most
useful to vital registration staff
members, NCHS requests information
from State and local vital registration
officials about their projected needs for
training. NCHS also asks individual
candidates for training to submit an
application form containing name,
address, occupation, work experience,
education, and previous training. These
data enable NCHS to determine those
individuals whose needs can best be
met through the available training
resources. NCHS is requesting 3 years of
OMB clearance for this project.
There is no cost to respondents in
providing these data.
clarity of the information to be
collected; and (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. Written comments should
be received within 60 days of this
notice.
Proposed Project
Vital Statistics Training Application,
(OMB No. 0920–0217 exp. 7/31/2010)—
Extension—National Center for Health
Statistics (NCHS), Centers for Disease
Control and Prevention (CDC).
Background and Brief Description
In the United States, legal authority
for the registration of vital events, i.e.,
births, deaths, marriages, divorces, fetal
deaths, and induced terminations of
pregnancy, resides individually with the
States (as well as cities in the case of
New York City and Washington, DC)
and Puerto Rico, the Virgin Islands,
Guam, American Samoa, and the
Commonwealth of the Northern Mariana
Islands. These governmental entities are
the full legal proprietors of vital records
and the information contained therein.
As a result of this State authority, the
collection of registration-based vital
statistics at the national level, referred
to as the U.S. National Vital Statistics
System (NVSS), depends on a
cooperative relationship between the
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents
Respondents
State, local, and Territory Registration Officials ..............................................
Training applicants ...........................................................................................
Number of
responses per
respondent
57
100
1
1
Total ..........................................................................................................
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
[FR Doc. 2010–510 Filed 1–12–10; 8:45 am]
[Docket No. FDA–2009–D–0605]
srobinson on DSKHWCL6B1PROD with NOTICES
Food and Drug Administration
Draft Guidance for Institutional Review
Boards, Clinical Investigators, and
Sponsors: IRB Continuing Review
After Clinical Investigation Approval;
Availability
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
SUMMARY: The Food and Drug
Administration (FDA) is announcing the
availability of a draft guidance entitled,
VerDate Nov<24>2008
16:51 Jan 12, 2010
Jkt 220001
PO 00000
Frm 00043
Fmt 4703
Sfmt 4703
20/60
15/60
Total burden
hours
19
25
44
Dated: January 7, 2010.
Maryam I. Daneshvar,
Acting Reports Clearance Officer, Centers for
Disease Control and Prevention.
BILLING CODE 4163–18–P
Average
burden per
response
(in hours)
‘‘Guidance for IRBs, Clinical
Investigators, and Sponsors: IRB
Continuing Review After Clinical
Investigation Approval.’’ The draft
guidance announced in this notice is
intended to assist institutional review
boards (IRBs) in carrying out their
continuing review responsibility by
providing recommendations regarding
the criteria, process, and frequency of
continuing review to assure the
protection of the rights and welfare of
subjects in clinical investigations. The
draft guidance should also help clinical
investigators and sponsors better
understand their responsibilities related
to continuing review.
E:\FR\FM\13JAN1.SGM
13JAN1
Agencies
[Federal Register Volume 75, Number 8 (Wednesday, January 13, 2010)]
[Notices]
[Page 1790]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2010-510]
[[Page 1790]]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[60Day-10-0217]
Proposed Data Collections Submitted for Public Comment and
Recommendations
In compliance with the requirement of Section 3506(c)(2)(A) of the
Paperwork Reduction Act of 1995 for opportunity for public comment on
proposed data collection projects, the Centers for Disease Control and
Prevention (CDC) will publish periodic summaries of proposed projects.
To request more information on the proposed projects or to obtain a
copy of the data collection plans and instruments, call 404-639-5960
and send comments to Maryam I. Daneshvar, CDC Acting Reports Clearance
Officer, 1600 Clifton Road, MS-D74, Atlanta, GA 30333 or send an e-mail
to omb@cdc.gov.
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; and (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. Written comments should be received
within 60 days of this notice.
Proposed Project
Vital Statistics Training Application, (OMB No. 0920-0217 exp. 7/
31/2010)--Extension--National Center for Health Statistics (NCHS),
Centers for Disease Control and Prevention (CDC).
Background and Brief Description
In the United States, legal authority for the registration of vital
events, i.e., births, deaths, marriages, divorces, fetal deaths, and
induced terminations of pregnancy, resides individually with the States
(as well as cities in the case of New York City and Washington, DC) and
Puerto Rico, the Virgin Islands, Guam, American Samoa, and the
Commonwealth of the Northern Mariana Islands. These governmental
entities are the full legal proprietors of vital records and the
information contained therein. As a result of this State authority, the
collection of registration-based vital statistics at the national
level, referred to as the U.S. National Vital Statistics System (NVSS),
depends on a cooperative relationship between the States and the
Federal government. This data collection, authorized by 42 U.S.C. 242k,
has been carried out by NCHS since it was created in 1960.
NCHS assists in achieving the comparability needed for combining
data from all States into national statistics, by conducting a training
program for State and local vital statistics staff to assist in
developing expertise in all aspects of vital registration and vital
statistics. The training offered under this program includes courses
for registration staff, statisticians, and coding specialists, all
designed to bring about a high degree of uniformity and quality in the
data provided by the States. This training program is authorized by 42
U.S.C. 242b, section 304(a). In order to offer the types of training
that would be most useful to vital registration staff members, NCHS
requests information from State and local vital registration officials
about their projected needs for training. NCHS also asks individual
candidates for training to submit an application form containing name,
address, occupation, work experience, education, and previous training.
These data enable NCHS to determine those individuals whose needs can
best be met through the available training resources. NCHS is
requesting 3 years of OMB clearance for this project.
There is no cost to respondents in providing these data.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Average
Number of Number of burden per Total burden
Respondents respondents responses per response (in hours
respondent hours)
----------------------------------------------------------------------------------------------------------------
State, local, and Territory Registration 57 1 20/60 19
Officials......................................
Training applicants............................. 100 1 15/60 25
---------------------------------------------------------------
Total....................................... .............. .............. .............. 44
----------------------------------------------------------------------------------------------------------------
Dated: January 7, 2010.
Maryam I. Daneshvar,
Acting Reports Clearance Officer, Centers for Disease Control and
Prevention.
[FR Doc. 2010-510 Filed 1-12-10; 8:45 am]
BILLING CODE 4163-18-P