Proposed Data Collections Submitted for Public Comment and Recommendations, 61426-61427 [E8-24568]
Download as PDF
61426
Federal Register / Vol. 73, No. 201 / Thursday, October 16, 2008 / Notices
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents
Type of respondent
Number of
responses per
respondent
Average burden
per response (in
hours)
Total burden
hours
1. Screener Respondents ................................................................
2. Interview respondents .................................................................
14,000
5,000
1
1
3/60
1.2
700
6,000
Total ..........................................................................................
............................
............................
............................
6,700
Dated: October 3, 2008.
Maryam I. Daneshvar,
Acting Reports Clearance Officer, Office of
the Chief Science Officer, Centers for Disease
Control and Prevention.
[FR Doc. E8–24561 Filed 10–15–08; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60 Day-08–0134]
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.
Alternatively, to obtain a copy of the
data collection plans and instrument,
call 404–639–5960 and send comments
to Maryam I. Daneshvar, CDC Reports
Clearance Officer, 1600 Clifton Road
NE., MS–D74, Atlanta, Georgia 30333;
comments may also be sent by 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 a
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 information technology. Written
comments should be received within 60
days of this notice.
Proposed Project
Foreign Quarantine Regulations (42
CFR part 71) (OMB Control No. 0920–
0134)—Revision—National Center for
Preparedness, Detection, and Control of
Infectious Diseases (NCPDCID), Centers
for Disease Control and Prevention
(CDC)
Background and Brief Description
Section 361 of the Public Health
Service Act (42 U.S.C. 264) authorizes
the Secretary of Health and Human
Services (HHS) to make and enforce
regulations necessary to prevent the
introduction, transmission, or spread of
communicable diseases from foreign
countries into the United States.
Legislation and the existing regulations
governing foreign quarantine activities
(42 CFR part 71) authorize quarantine
officers and other personnel to inspect
and undertake control measures with
respect to conveyances, persons, and
shipments of animals and etiologic
agents entering the United States from
foreign ports in order to protect the
public health.
Under foreign quarantine regulations,
the master of a ship or commander of an
airplane entering the United States from
a foreign port is required by public
health law to report certain illnesses
among passengers (42 CFR 71.21(b)).
CDC recently reviewed 42 CFR part 71
and determined that five data collection
requirements and one recordkeeping
requirement had not been included in
previous information collection request
submissions. Thus, in this request to
OMB, CDC is requesting approval for an
additional 2,902 burden hours.
The first additional data collection
requirement is the designation of yellow
fever vaccination clinics. Under 42 CFR
71.3, the Director of CDC delegates to
states the responsibility for designation
of yellow fever vaccination clinics to
states and territories. States and
territories then designate the clinics,
based on application by the facilities
and presentation of evidence. Under the
regulation, facilities must provide
evidence of adequate facilities and
professionally trained personnel for
handling, storage, and administration of
the vaccine. The designated center must
also comply with any instruction issued
by the CDC Director for handling,
storage, and administration of the
vaccine. CDC estimates that
approximately 500 professional staff are
added each year as a registered stamp
holder for the International Certificate of
Vaccination or Prophylaxis. The
estimated time to gather records and
apply to become a stamp holder is one
hour. The additional burden for this
provision is 500 hours.
The second additional data collection
requirement is found in 42 CFR
71.55(c). This provision requires that
the remains of a person who died of a
communicable disease listed in
§ 71.32(b) may not be brought back into
a U.S. port unless the body is (a)
Properly embalmed and placed in a
hermetically sealed casket, (b) cremated,
or (c) accompanied by a permit issued
by the Director of CDC. CDC has
determined that the issuance of a permit
implies a data collection requirement.
CDC estimates a maximum of 5
respondents annually with an average
burden of one hour per respondent, for
an increase of 5 hours for this provision.
The last three data collection
requirements are found under § 71.56.
CDC established this section by Interim
Final Rule in 2003 (68 FR 62353). This
section prohibits the importation of
African rodents, or any rodents whose
native habitat is Africa, or any products
derived from such rodents. Those
wishing to import such animals or
products may apply to the Director of
CDC for an exemption to this
prohibition and may appeal the
Director’s decision. Finally, an
individual or company may appeal a
CDC order causing an animal to be
quarantined, re-exported or destroyed.
These data collection requirements were
originally approved by OMB under
OMB Control No. 0920–0615. This
approval expired July 31, 2004.
Although CDC collected data from less
than 9 respondents annually since the
Interim Final Rule went into effect, CDC
wishes to reinstate the data collection
requirement following recent review of
42 CFR 71. This reinstatement is for 22
burden hours.
Finally, § 71.21(c) requires reporting
of the number of cases (including zero)
of gastrointestinal illness in passengers
and crew recorded in the ship’s medical
log during the current cruise. CDC had
already included the reporting
61427
Federal Register / Vol. 73, No. 201 / Thursday, October 16, 2008 / Notices
requirement in its information
collection request, but had not included
the recordkeeping requirement of the
medical log. In addition, CDC is
changing the requirement from
reporting gastrointestinal illness to
reporting all diseases of public health
significance. This submission includes
the medical log recordkeeping
requirement, for an additional 2,375
burden hours.
Respondents include airline pilots,
ships’ captains, importers, medical
professionals, and travelers. The nature
of the quarantine response dictates
which forms are completed by whom.
There are no costs to respondents
except their time to complete the forms.
ESTIMATE OF ANNUALIZED BURDEN HOURS
Number of
respondents
Citation
Responses per
respondent
Average burden
per respondent
(in hours)
Total burden
(in hours)
71.21 Radio report death/illness ...................................................
71.21(c) Medical log ......................................................................
71.3 Designation of yellow fever vaccination centers ...................
71.33(c) Report by person(s) in isolation or surveillance .............
71.35 Report of death/illness in port .............................................
Outbreak of public health significance ............................................
Reporting of ill passenger(s) ...........................................................
71.51(b)(3) Admission of cats/dogs; death/illness ........................
71.51(d) Dogs/cats; certification of confinement, vaccination .......
71.52(d) Turtle importation permits ...............................................
71.53(d) Importer registration—nonhuman primates ....................
71.53(d) Recordkeeping ................................................................
71.55 Permit for dead body ..........................................................
71.56(a)(ii) Request for exemption ...............................................
71.56(a)(iii) Appeal ........................................................................
71.56(c) Appeal .............................................................................
9,500
9,500
500
11
5
2,700,000
800
5
1,200
10
40
30
5
12
5
5
1
1
1
1
1
1
1
1
1
1
1
4
1
1
1
1
2/60
15/60
1
3/60
30/60
5/60
5/60
3/60
15/60
30/60
10/60
30/60
1
1
1
1
317
2,375
500
1
3
225,000
67
1
300
5
67
60
5
12
5
5
Total ..........................................................................................
............................
............................
............................
228,723
Dated: October 1, 2008.
Maryam I. Daneshvar,
Reports Clearance Officer, Centers for Disease
Control and Prevention.
[FR Doc. E8–24568 Filed 10–15–08; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
Healthcare Infection Control Practices
Advisory Committee, (HICPAC)
In accordance with section 10(a)(2) of
the Federal Advisory Committee Act
(Pub. L. 92–463), the Centers for Disease
Control and Prevention (CDC)
announces the following meeting for the
aforementioned committee:
Times and Dates:
9 a.m.–5 p.m., November 13, 2008.
9 a.m.–1 p.m., November 14, 2008.
Place: The Washington Marriott, 1221
22nd Street, NW., Washington, DC 20037.
Status: Open to the public, limited only by
the space available.
Purpose: The Committee is charged with
providing advice and guidance to the
Secretary, the Assistant Secretary for Health,
the Director, CDC, and the Director, National
Center for Preparedness, Detection, and
Control of Infectious Diseases (NCPDCID),
regarding (1) The practice of hospital
infection control; (2) Strategies for
surveillance, prevention, and control of
infections (e.g., nosocomial infections),
antimicrobial resistance, and related events
in settings where healthcare is provided; and
(3) Periodic updating of guidelines and other
policy statements regarding prevention of
healthcare-associated infections and
healthcare-related conditions.
Matters To Be Discussed: The agenda will
include a follow-up discussion of Health and
Human Services Healthcare-Associated
Infections Elimination Process, Urinary Tract
Infections Guideline, and Norovirus
Guideline.
Agenda items are subject to change as
priorities dictate.
Contact Person for More Information:
Wendy Vance, HICPAC, Division of
Healthcare Quality Promotion, NCPDCID,
CDC, l600 Clifton Road, NE., Mailstop D–10,
Atlanta, Georgia 30333 Telephone (404) 639–
2891.
The Director, Management Analysis and
Services Office, has been delegated the
authority to sign Federal Register notices
pertaining to announcements of meetings and
other committee management activities, for
both CDC and the Agency for Toxic
Substances and Disease Registry.
Dated: October 7, 2008.
Elaine L. Baker,
Director, Management Analysis and Services
Office, Centers for Disease Control and
Prevention (CDC).
[FR Doc. E8–24563 Filed 10–15–08; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
National Center for Injury Prevention
and Control/ Initial Review Group,
(NCIPC/IRG)
In accordance with section 10(a)(2) of
the Federal Advisory Committee Act
(Pub. L. 92–463), the Centers for Disease
Control and Prevention (CDC)
announces the following meeting of the
aforementioned review group:
Times and Dates:
7 p.m.–8 p.m., November 18, 2008 (Open).
7:45 a.m.–5 p.m., November 19, 2008
(Closed).
7:45 a.m.–5 p.m., November 20, 2008
(Closed).
7:45 a.m.–5 p.m., November 21, 2008
(Closed).
Place: The W Hotel, 3377 Peachtree Road,
NE., Atlanta, Georgia 30326, Telephone:
(678) 500–3181.
Status: Portions of the meetings will be
closed to the public in accordance with
provisions set forth in Section 552b(c)(4) and
(6), Title 5, U.S.C., and the Determination of
the Director, Management Analysis and
Services Office, CDC, pursuant to Section
10(d) of Public Law 92–463.
Purpose: This group is charged with
providing advice and guidance to the
Secretary, Department of Health and Human
Services, and the Director, CDC, concerning
the scientific and technical merit of grant and
cooperative agreement applications received
Agencies
[Federal Register Volume 73, Number 201 (Thursday, October 16, 2008)]
[Notices]
[Pages 61426-61427]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E8-24568]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[60 Day-08-0134]
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.
Alternatively, to obtain a copy of the data collection plans and
instrument, call 404-639-5960 and send comments to Maryam I. Daneshvar,
CDC Reports Clearance Officer, 1600 Clifton Road NE., MS-D74, Atlanta,
Georgia 30333; comments may also be sent by 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 a 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 information technology. Written comments
should be received within 60 days of this notice.
Proposed Project
Foreign Quarantine Regulations (42 CFR part 71) (OMB Control No.
0920-0134)--Revision--National Center for Preparedness, Detection, and
Control of Infectious Diseases (NCPDCID), Centers for Disease Control
and Prevention (CDC)
Background and Brief Description
Section 361 of the Public Health Service Act (42 U.S.C. 264)
authorizes the Secretary of Health and Human Services (HHS) to make and
enforce regulations necessary to prevent the introduction,
transmission, or spread of communicable diseases from foreign countries
into the United States. Legislation and the existing regulations
governing foreign quarantine activities (42 CFR part 71) authorize
quarantine officers and other personnel to inspect and undertake
control measures with respect to conveyances, persons, and shipments of
animals and etiologic agents entering the United States from foreign
ports in order to protect the public health.
Under foreign quarantine regulations, the master of a ship or
commander of an airplane entering the United States from a foreign port
is required by public health law to report certain illnesses among
passengers (42 CFR 71.21(b)). CDC recently reviewed 42 CFR part 71 and
determined that five data collection requirements and one recordkeeping
requirement had not been included in previous information collection
request submissions. Thus, in this request to OMB, CDC is requesting
approval for an additional 2,902 burden hours.
The first additional data collection requirement is the designation
of yellow fever vaccination clinics. Under 42 CFR 71.3, the Director of
CDC delegates to states the responsibility for designation of yellow
fever vaccination clinics to states and territories. States and
territories then designate the clinics, based on application by the
facilities and presentation of evidence. Under the regulation,
facilities must provide evidence of adequate facilities and
professionally trained personnel for handling, storage, and
administration of the vaccine. The designated center must also comply
with any instruction issued by the CDC Director for handling, storage,
and administration of the vaccine. CDC estimates that approximately 500
professional staff are added each year as a registered stamp holder for
the International Certificate of Vaccination or Prophylaxis. The
estimated time to gather records and apply to become a stamp holder is
one hour. The additional burden for this provision is 500 hours.
The second additional data collection requirement is found in 42
CFR 71.55(c). This provision requires that the remains of a person who
died of a communicable disease listed in Sec. 71.32(b) may not be
brought back into a U.S. port unless the body is (a) Properly embalmed
and placed in a hermetically sealed casket, (b) cremated, or (c)
accompanied by a permit issued by the Director of CDC. CDC has
determined that the issuance of a permit implies a data collection
requirement. CDC estimates a maximum of 5 respondents annually with an
average burden of one hour per respondent, for an increase of 5 hours
for this provision.
The last three data collection requirements are found under Sec.
71.56. CDC established this section by Interim Final Rule in 2003 (68
FR 62353). This section prohibits the importation of African rodents,
or any rodents whose native habitat is Africa, or any products derived
from such rodents. Those wishing to import such animals or products may
apply to the Director of CDC for an exemption to this prohibition and
may appeal the Director's decision. Finally, an individual or company
may appeal a CDC order causing an animal to be quarantined, re-exported
or destroyed. These data collection requirements were originally
approved by OMB under OMB Control No. 0920-0615. This approval expired
July 31, 2004. Although CDC collected data from less than 9 respondents
annually since the Interim Final Rule went into effect, CDC wishes to
reinstate the data collection requirement following recent review of 42
CFR 71. This reinstatement is for 22 burden hours.
Finally, Sec. 71.21(c) requires reporting of the number of cases
(including zero) of gastrointestinal illness in passengers and crew
recorded in the ship's medical log during the current cruise. CDC had
already included the reporting
[[Page 61427]]
requirement in its information collection request, but had not included
the recordkeeping requirement of the medical log. In addition, CDC is
changing the requirement from reporting gastrointestinal illness to
reporting all diseases of public health significance. This submission
includes the medical log recordkeeping requirement, for an additional
2,375 burden hours.
Respondents include airline pilots, ships' captains, importers,
medical professionals, and travelers. The nature of the quarantine
response dictates which forms are completed by whom.
There are no costs to respondents except their time to complete the
forms.
Estimate of Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Average burden
Citation Number of Responses per per respondent Total burden (in
respondents respondent (in hours) hours)
----------------------------------------------------------------------------------------------------------------
71.21 Radio report death/illness........ 9,500 1 2/60 317
71.21(c) Medical log.................... 9,500 1 15/60 2,375
71.3 Designation of yellow fever 500 1 1 500
vaccination centers....................
71.33(c) Report by person(s) in 11 1 3/60 1
isolation or surveillance..............
71.35 Report of death/illness in port... 5 1 30/60 3
Outbreak of public health significance.. 2,700,000 1 5/60 225,000
Reporting of ill passenger(s)........... 800 1 5/60 67
71.51(b)(3) Admission of cats/dogs; 5 1 3/60 1
death/illness..........................
71.51(d) Dogs/cats; certification of 1,200 1 15/60 300
confinement, vaccination...............
71.52(d) Turtle importation permits..... 10 1 30/60 5
71.53(d) Importer registration--nonhuman 40 1 10/60 67
primates...............................
71.53(d) Recordkeeping.................. 30 4 30/60 60
71.55 Permit for dead body.............. 5 1 1 5
71.56(a)(ii) Request for exemption...... 12 1 1 12
71.56(a)(iii) Appeal.................... 5 1 1 5
71.56(c) Appeal......................... 5 1 1 5
-----------------------------------------------------------------------
Total............................... ................ ................ ................ 228,723
----------------------------------------------------------------------------------------------------------------
Dated: October 1, 2008.
Maryam I. Daneshvar,
Reports Clearance Officer, Centers for Disease Control and Prevention.
[FR Doc. E8-24568 Filed 10-15-08; 8:45 am]
BILLING CODE 4163-18-P