Agency Forms Undergoing Paperwork Reduction Act Review, 49373-49374 [2020-17709]
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Federal Register / Vol. 85, No. 157 / Thursday, August 13, 2020 / Notices
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30Day–20–0263]
Agency Forms Undergoing Paperwork
Reduction Act Review
In accordance with the Paperwork
Reduction Act of 1995, the Centers for
Disease Control and Prevention (CDC)
has submitted the information
collection request titled Requirements
for the Importation of Nonhuman
Primates into the United States to the
Office of Management and Budget
(OMB) for review and approval. CDC
previously published a ‘‘Proposed Data
Collection Submitted for Public
Comment and Recommendations’’
notice on December 6, 2019 to obtain
comments from the public and affected
agencies. CDC received six comments
related to the previous notice. This
notice serves to allow an additional 30
days for public and affected agency
comments.
CDC will accept all comments for this
proposed information collection project.
The Office of Management and Budget
is particularly interested in comments
that:
(a) Evaluate whether the proposed
collection of information is necessary
for the proper performance of the
functions of the agency, including
whether the information will have
practical utility;
(b) Evaluate the accuracy of the
agencies estimate of the burden of the
proposed collection of information,
including the validity of the
methodology and assumptions used;
(c) Enhance the quality, utility, and
clarity of the information to be
collected;
(d) Minimize the burden of the
collection of information on those who
are to respond, including, through the
use of appropriate automated,
electronic, mechanical, or other
technological collection techniques or
other forms of information technology,
e.g., permitting electronic submission of
responses; and
(e) Assess information collection
costs.
To request additional information on
the proposed project or to obtain a copy
of the information collection plan and
instruments, call (404) 639–7570.
Comments and recommendations for the
proposed information collection should
be sent within 30 days of publication of
this notice to www.reginfo.gov/public/
do/PRAMain. Find this particular
information collection by selecting
VerDate Sep<11>2014
17:16 Aug 12, 2020
Jkt 250001
‘‘Currently under 30-day Review—Open
for Public Comments’’ or by using the
search function. Direct written
comments and/or suggestions regarding
the items contained in this notice to the
Attention: CDC Desk Officer, Office of
Management and Budget, 725 17th
Street NW, Washington, DC 20503 or by
fax to (202) 395–5806. Provide written
comments within 30 days of notice
publication.
Proposed Project
Requirements for the Importation of
Nonhuman Primates into the United
States (OMB Control No. 0920–0263,
Exp. 08/31/2020)—Revision—National
Center for Emerging and Zoonotic
Infectious Diseases (NCEZID), Centers
for Disease Control and Prevention
(CDC).
Background and Brief Description
Under 42 CFR 71.53, CDC collects
information pertaining to importers and
imported nonhuman primates (NHP).
This information collection enables CDC
to evaluate compliance with pre-arrival
of shipment notification requirements,
to investigate the number and species of
imported nonhuman primates, and to
determine if adequate measures being
taken for the prevention of exposure to
persons and animals during
importation.
Since May 1990, CDC has monitored
the arrival and/or uncrating of certain
shipments of non-human primates
imported into the United States. In
February 2013, CDC promulgated two
regulations pertaining to the
importation of nonhuman primates. The
first rule, Establishment of User Fees for
Filovirus Testing of Nonhuman Primate
Liver Samples, outlines a process by
which importers can send liver tissues
to CDC from primates that die during
importation from reasons other than
trauma (2/12/2013, Vol.78, No. 29, p.
9828). CDC performs these tests due to
the absence of a private sector option.
The second rule, Requirements for
Importers of Nonhuman Primates,
consolidates into 42 CFR 71.53 the
requirements previously found in 42
CFR part 71.53 with those found in the
Special Permit to Import Cynomolgus,
African Green, or Rhesus Monkeys into
the United States (2/15/2013, Vol. 78,
No. 32/p. 11522). It also rescinded the
six-month special-permit requirements
for cynomolgus, African green, and
rhesus monkeys and extended the time
period for registration/permit renewal
from 180 days to two years, reducing
much of the respondent burden. CDC
feels these regulatory changes and
reporting requirements balance the
public health risks posed by the
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Fmt 4703
Sfmt 4703
49373
importation of nonhuman primates with
the burden imposed on regulating their
importation.
This information collection is
designed to support real-time regulatory
and monitoring activities, and the
prevention of disease transmission from
NHP to humans. Therefore, there is no
standard reporting deadline or
frequency. Respondents are only
required to provide the information
under the regulation if they seek to
import nonhuman primates in the
United States.
The CDC is requesting approval for a
set of adjustments to the previously
approved burden total for this
information collection. The adjustments
are as follows:
Adjustments
Based on the number of registered
importers processed by CDC, CDC is
adjusting upward, two of the
information collections within this
submission:
• Nonhuman Primate Importer
Recordkeeping and reporting
requirements for importing NHPs:
Notification of shipment arrival
71.53(n).
• Nonhuman Primate Importer
Quarantine release 71.53(l).
Changes
CDC is proposing a reformatting and
changes to CDC 75.10A Registration
Form for NHP Importation to clarify for
respondents the information that should
be submitted. This results in no changes
in respondent burden.
CDC is adding the following
information collections to delineate
between specific information collections
under the regulations at 42 CFR
71.53(m):
• Statements regarding the health of
the nonhuman primates during travel
and CDC quarantine (42 CFR 71.53(m)
(no form)
• Statements, including necropsy
reports, about the nonhuman primates
upon their release from CDC quarantine.
(42 CFR 71.53(m)
CDC is removing information
collections, because CDC is not using
the Partner Government Agency
Message Set functionality within the
Automated Commercial Environment:
• CDC Partner Government Agency
Message Set for Importing Live
Nonhuman Primates
• CDC Partner Government Agency
Message Set for Importing Nonhuman
Primate Products
• Documentation of Non-infectiousness
71.53(t)
OMB approval is requested for three
years. The total number of hours
E:\FR\FM\13AUN1.SGM
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49374
Federal Register / Vol. 85, No. 157 / Thursday, August 13, 2020 / Notices
requested for this information collection
total 185, which is a decrease of 737
hours.
ESTIMATED ANNUALIZED BURDEN HOURS
Form name/CFR reference
Nonhuman Primate Importer ..
CDC 75.10A Application for Registration as an Importer of
Nonhuman Primates (New Importer).
CDC 75.10A Application for Registration as an Importer of
Nonhuman Primates (Re-Registration).
71.53(g1)(iii) and (h) Documentation and Standard Operating Procedures (no form) (New Importer).
71.53(g)(1)(iii) and (h) Documentation and Standard Operating Procedures (no form) (Registered Importer).
Recordkeeping and reporting requirements for importing
NHPs: Notification of shipment arrival 71.53(k), (n) (no
form).
Statements regarding the health of the nonhuman primates
during travel and CDC quarantine (42 CFR 71.53(m) (no
form).
Statements, including necropsy reports, about the
nonhuman primates upon their release from CDC quarantine. (42 CFR 71.53(m) (no form).
Quarantine release 71.53(l) (no form) ...................................
71.53(v) Form: Filovirus Diagnostic Specimen Submission
Form for Non-human Primate Materials.
Nonhuman Primate Importer ..
Nonhuman Primate Importer ..
Nonhuman Primate Importer ..
Nonhuman Primate Importer ..
Nonhuman Primate Importer ..
Nonhuman Primate Importer ..
Nonhuman Primate Importer ..
Nonhuman Primate Importer ..
Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Scientific Integrity, Office of Science,
Centers for Disease Control and Prevention.
[FR Doc. 2020–17709 Filed 8–12–20; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–20–1054; Docket No. CDC–2020–
0090]
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 a proposed information
collection entitled ‘‘Drug Overdose
Response Investigation (DORI) Data
Collections.’’ CDC will use the
SUMMARY:
VerDate Sep<11>2014
17:16 Aug 12, 2020
Jkt 250001
information collected to respond to
urgent requests from state and local
health authorities to provide
epidemiological information that allows
for the selection of interventions to curb
local epidemics of drug overdose.
DATES: Written comments must be
received on or before October 13, 2020.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2020–
0090 by any of the following methods:
• Federal eRulemaking Portal:
Regulations.gov. Follow the instructions
for submitting comments.
• Mail: Jeffrey M. Zirger, 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. CDC will post, without
change, all relevant comments to
Regulations.gov.
Please note: Submit all comments
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 Jeffrey M. Zirger,
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.
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Frm 00016
Fmt 4703
Sfmt 4703
Number of
responses per
respondent
Number of
respondents
Type of respondent
Average
burden per
response
(in hours)
1
1
10/60
12
1
10/60
1
1
10
12
1
30/60
25
6
15/60
25
6
15/60
25
3
15/60
25
10
6
10
15/60
20/60
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 the OMB for approval. To
comply with this requirement, we are
publishing this notice of a proposed
data collection as described below.
The OMB is particularly interested in
comments that will help:
1. Evaluate whether the proposed
collection of information is necessary
for the proper performance of the
functions of the agency, including
whether the information will have
practical utility;
2. Evaluate the accuracy of the
agency’s estimate of the burden of the
proposed collection of information,
including the validity of the
methodology and assumptions used;
3. Enhance the quality, utility, and
clarity of the information to be
collected; and
4. Minimize the burden of the
collection of information on those who
are to respond, including through the
SUPPLEMENTARY INFORMATION:
E:\FR\FM\13AUN1.SGM
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]]>Agencies
[Federal Register Volume 85, Number 157 (Thursday, August 13, 2020)]
[Notices]
[Pages 49373-49374]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2020-17709]
[[Page 49373]]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[30Day-20-0263]
Agency Forms Undergoing Paperwork Reduction Act Review
In accordance with the Paperwork Reduction Act of 1995, the Centers
for Disease Control and Prevention (CDC) has submitted the information
collection request titled Requirements for the Importation of Nonhuman
Primates into the United States to the Office of Management and Budget
(OMB) for review and approval. CDC previously published a ``Proposed
Data Collection Submitted for Public Comment and Recommendations''
notice on December 6, 2019 to obtain comments from the public and
affected agencies. CDC received six comments related to the previous
notice. This notice serves to allow an additional 30 days for public
and affected agency comments.
CDC will accept all comments for this proposed information
collection project. The Office of Management and Budget is particularly
interested in comments that:
(a) Evaluate whether the proposed collection of information is
necessary for the proper performance of the functions of the agency,
including whether the information will have practical utility;
(b) Evaluate the accuracy of the agencies estimate of the burden of
the proposed collection of information, including the validity of the
methodology and assumptions used;
(c) Enhance the quality, utility, and clarity of the information to
be collected;
(d) Minimize the burden of the collection of information on those
who are to respond, including, through the use of appropriate
automated, electronic, mechanical, or other technological collection
techniques or other forms of information technology, e.g., permitting
electronic submission of responses; and
(e) Assess information collection costs.
To request additional information on the proposed project or to
obtain a copy of the information collection plan and instruments, call
(404) 639-7570. Comments and recommendations for the proposed
information collection should be sent within 30 days of publication of
this notice to www.reginfo.gov/public/do/PRAMain. Find this particular
information collection by selecting ``Currently under 30-day Review--
Open for Public Comments'' or by using the search function. Direct
written comments and/or suggestions regarding the items contained in
this notice to the Attention: CDC Desk Officer, Office of Management
and Budget, 725 17th Street NW, Washington, DC 20503 or by fax to (202)
395-5806. Provide written comments within 30 days of notice
publication.
Proposed Project
Requirements for the Importation of Nonhuman Primates into the
United States (OMB Control No. 0920-0263, Exp. 08/31/2020)--Revision--
National Center for Emerging and Zoonotic Infectious Diseases (NCEZID),
Centers for Disease Control and Prevention (CDC).
Background and Brief Description
Under 42 CFR 71.53, CDC collects information pertaining to
importers and imported nonhuman primates (NHP). This information
collection enables CDC to evaluate compliance with pre-arrival of
shipment notification requirements, to investigate the number and
species of imported nonhuman primates, and to determine if adequate
measures being taken for the prevention of exposure to persons and
animals during importation.
Since May 1990, CDC has monitored the arrival and/or uncrating of
certain shipments of non-human primates imported into the United
States. In February 2013, CDC promulgated two regulations pertaining to
the importation of nonhuman primates. The first rule, Establishment of
User Fees for Filovirus Testing of Nonhuman Primate Liver Samples,
outlines a process by which importers can send liver tissues to CDC
from primates that die during importation from reasons other than
trauma (2/12/2013, Vol.78, No. 29, p. 9828). CDC performs these tests
due to the absence of a private sector option. The second rule,
Requirements for Importers of Nonhuman Primates, consolidates into 42
CFR 71.53 the requirements previously found in 42 CFR part 71.53 with
those found in the Special Permit to Import Cynomolgus, African Green,
or Rhesus Monkeys into the United States (2/15/2013, Vol. 78, No. 32/p.
11522). It also rescinded the six-month special-permit requirements for
cynomolgus, African green, and rhesus monkeys and extended the time
period for registration/permit renewal from 180 days to two years,
reducing much of the respondent burden. CDC feels these regulatory
changes and reporting requirements balance the public health risks
posed by the importation of nonhuman primates with the burden imposed
on regulating their importation.
This information collection is designed to support real-time
regulatory and monitoring activities, and the prevention of disease
transmission from NHP to humans. Therefore, there is no standard
reporting deadline or frequency. Respondents are only required to
provide the information under the regulation if they seek to import
nonhuman primates in the United States.
The CDC is requesting approval for a set of adjustments to the
previously approved burden total for this information collection. The
adjustments are as follows:
Adjustments
Based on the number of registered importers processed by CDC, CDC
is adjusting upward, two of the information collections within this
submission:
Nonhuman Primate Importer Recordkeeping and reporting
requirements for importing NHPs: Notification of shipment arrival
71.53(n).
Nonhuman Primate Importer Quarantine release 71.53(l).
Changes
CDC is proposing a reformatting and changes to CDC 75.10A
Registration Form for NHP Importation to clarify for respondents the
information that should be submitted. This results in no changes in
respondent burden.
CDC is adding the following information collections to delineate
between specific information collections under the regulations at 42
CFR 71.53(m):
Statements regarding the health of the nonhuman primates
during travel and CDC quarantine (42 CFR 71.53(m) (no form)
Statements, including necropsy reports, about the nonhuman
primates upon their release from CDC quarantine. (42 CFR 71.53(m)
CDC is removing information collections, because CDC is not using
the Partner Government Agency Message Set functionality within the
Automated Commercial Environment:
CDC Partner Government Agency Message Set for Importing Live
Nonhuman Primates
CDC Partner Government Agency Message Set for Importing
Nonhuman Primate Products
Documentation of Non-infectiousness 71.53(t)
OMB approval is requested for three years. The total number of
hours
[[Page 49374]]
requested for this information collection total 185, which is a
decrease of 737 hours.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Average
Number of Number of burden per
Type of respondent Form name/CFR reference respondents responses per response (in
respondent hours)
----------------------------------------------------------------------------------------------------------------
Nonhuman Primate Importer.......... CDC 75.10A Application for 1 1 10/60
Registration as an
Importer of Nonhuman
Primates (New Importer).
Nonhuman Primate Importer.......... CDC 75.10A Application for 12 1 10/60
Registration as an
Importer of Nonhuman
Primates (Re-Registration).
Nonhuman Primate Importer.......... 71.53(g1)(iii) and (h) 1 1 10
Documentation and Standard
Operating Procedures (no
form) (New Importer).
Nonhuman Primate Importer.......... 71.53(g)(1)(iii) and (h) 12 1 30/60
Documentation and Standard
Operating Procedures (no
form) (Registered
Importer).
Nonhuman Primate Importer.......... Recordkeeping and reporting 25 6 15/60
requirements for importing
NHPs: Notification of
shipment arrival 71.53(k),
(n) (no form).
Nonhuman Primate Importer.......... Statements regarding the 25 6 15/60
health of the nonhuman
primates during travel and
CDC quarantine (42 CFR
71.53(m) (no form).
Nonhuman Primate Importer.......... Statements, including 25 3 15/60
necropsy reports, about
the nonhuman primates upon
their release from CDC
quarantine. (42 CFR
71.53(m) (no form).
Nonhuman Primate Importer.......... Quarantine release 71.53(l) 25 6 15/60
(no form).
Nonhuman Primate Importer.......... 71.53(v) Form: Filovirus 10 10 20/60
Diagnostic Specimen
Submission Form for Non-
human Primate Materials.
----------------------------------------------------------------------------------------------------------------
Jeffrey M. Zirger,
Lead, Information Collection Review Office, Office of Scientific
Integrity, Office of Science, Centers for Disease Control and
Prevention.
[FR Doc. 2020-17709 Filed 8-12-20; 8:45 am]
BILLING CODE 4163-18-P
