Agency Information Collection Activities; Proposed eCollection eComments Requested; Revision of a Currently Approved Collection Bioterrorism Preparedness Act: Entity/Individual Information, 12207-12208 [2021-04208]
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jbell on DSKJLSW7X2PROD with NOTICES
Federal Register / Vol. 86, No. 39 / Tuesday, March 2, 2021 / Notices
6, 10, 12, and 13 of the ’007 patent; and
whether an industry in the United
States exists as required by subsection
(a)(2) of section 337;
(2) Pursuant to section 210.10(b)(1) of
the Commission’s Rules of Practice and
Procedure, 19 CFR 210.10(b)(1), the
plain language description of the
accused products or category of accused
products, which defines the scope of the
investigation, is ‘‘robotic vacuums and
wet/dry mops, their docking stations,
and associated parts and components
(including software)’’;
(3) For the purpose of the
investigation so instituted, the following
are hereby named as parties upon which
this notice of investigation shall be
served:
(a) The complainant is:
iRobot Corporation
8 Crosby Drive
Bedford, MA 01730
(b) The respondents are the following
entities alleged to be in violation of
section 337, and are the parties upon
which the complaint is to be served:
SharkNinja Operating LLC, 89 A St.
#100, Needham, MA 02494
SharkNinja Management LLC, 89 A St.
#100, Needham, MA 02494
SharkNinja Management Co., 89 A St.
#100, Needham, MA 02494
SharkNinja Sales Co., 89 A St. #100,
Needham, MA 02494
EP Midco LLC, 89 A St. #100, Needham,
MA 02494
SharkNinja Hong Kong Co. Ltd., 238 Des
Voeux Road Central, Sheung Wan,
Central & Western District—Hong
Kong Island, Hong Kong
(4) For the investigation so instituted,
the Chief Administrative Law Judge,
U.S. International Trade Commission,
shall designate the presiding
Administrative Law Judge.
The Office of Unfair Import
Investigations will not participate as a
party in this investigation.
Responses to the complaint and the
notice of investigation must be
submitted by the named respondents in
accordance with section 210.13 of the
Commission’s Rules of Practice and
Procedure, 19 CFR 210.13. Pursuant to
19 CFR 201.16(e) and 210.13(a), as
amended in 85 FR 15798 (March 19,
2020), such responses will be
considered by the Commission if
received not later than 20 days after the
date of service by the complainant of the
complaint and the notice of
investigation. Extensions of time for
submitting responses to the complaint
and the notice of investigation will not
be granted unless good cause therefor is
shown.
Failure of a respondent to file a timely
response to each allegation in the
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complaint and in this notice may be
deemed to constitute a waiver of the
right to appear and contest the
allegations of the complaint and this
notice, and to authorize the
administrative law judge and the
Commission, without further notice to
the respondent, to find the facts to be as
alleged in the complaint and this notice
and to enter an initial determination
and a final determination containing
such findings, and may result in the
issuance of an exclusion order or a cease
and desist order or both directed against
the respondent.
By order of the Commission.
Issued: February 25, 2021.
Lisa Barton,
Secretary to the Commission.
[FR Doc. 2021–04294 Filed 3–1–21; 8:45 am]
BILLING CODE 7020–02–P
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
[Docket No. DEA–801]
Importer of Controlled Substances
Application: Stepan Company
Drug Enforcement
Administration, Justice.
ACTION: Notice of application.
AGENCY:
In
accordance with 21 CFR 1301.34(a), this
is notice that on February 08, 2021,
Stepan Company, 100 West Hunter
Avenue, Maywood, New Jersey 07607–
1021, applied to be registered as an
importer of the following basic class(es)
of controlled substance(s):
SUPPLEMENTARY INFORMATION:
Controlled
substance
Drug Code
Coca Leaves ....
9040
Schedule
II
The company plans to import the
listed controlled substance in bulk for
the manufacture of controlled
substances for distribution to its
customers. No other activity for this
drug code is authorized for this
registration.
Approval of permit applications will
occur only when the registrant’s
business activity is consistent with what
is authorized under 21 U.S.C. 952(a)(2).
Authorization will not extend to the
import of Food and Drug
Administration-approved or nonapproved finished dosage forms for
commercial sale.
William T. McDermott,
Assistant Administrator.
[FR Doc. 2021–04245 Filed 3–1–21; 8:45 am]
BILLING CODE 4410–09–P
Stepan Company has applied
to be registered as an importer of basic
class(es) of controlled substance(s).
Refer to Supplemental Information
listed below for further drug
information.
DATES: Registered bulk manufacturers of
the affected basic class(es), and
applicants therefore, may file written
comments on or objections to the
issuance of the proposed registration on
or before April 1, 2021. Such persons
may also file a written request for a
hearing on the application on or before
April 1, 2021.
ADDRESSES: Written comments should
be sent to: Drug Enforcement
Administration, Attention: DEA Federal
Register Representative/DPW, 8701
Morrissette Drive, Springfield, Virginia
22152. All requests for a hearing must
be sent to: Drug Enforcement
Administration, Attn: Administrator,
8701 Morrissette Drive, Springfield,
Virginia 22152. All requests for a
hearing should also be sent to: (1) Drug
Enforcement Administration, Attn:
Hearing Clerk/OALJ, 8701 Morrissette
Drive, Springfield, Virginia 22152; and
(2) Drug Enforcement Administration,
Attn: DEA Federal Register
Representative/DPW, 8701 Morrissette
Drive, Springfield, Virginia 22152.
SUMMARY:
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DEPARTMENT OF JUSTICE
Federal Bureau of Investigation
[OMB Number 1110–0039]
Agency Information Collection
Activities; Proposed eCollection
eComments Requested; Revision of a
Currently Approved Collection
Bioterrorism Preparedness Act: Entity/
Individual Information
Federal Bureau of
Investigation, Criminal Justice
Information Services Division,
Department of Justice.
ACTION: 60-Day notice.
AGENCY:
The Department of Justice
(DOJ), Federal Bureau of Investigation
(FBI), Criminal Justice Information
Services (CJIS) Division will be
submitting the following information
collection request to the Office of
Management and Budget (OMB) for
review and approval in accordance with
the Paperwork Reduction Act of 1995.
The proposed information collection is
published to obtain comments from the
public and affected agencies.
DATES: Comments are encouraged and
will be accepted for 60 days until May
3, 2021.
SUMMARY:
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Federal Register / Vol. 86, No. 39 / Tuesday, March 2, 2021 / Notices
If
you have additional comments
especially on the estimated public
burden or associated response time,
suggestions, or need a copy of the
proposed information collection
instrument with instructions or
additional information, please contact
James J. Sheets, Biometric Services
Section, Identity Management Unit,
Federal Bureau of Investigation, CJIS
Division, Biometric Technology Center,
1000 Custer Hollow Road, Clarksburg,
West Virginia 26306.
SUPPLEMENTARY INFORMATION: Written
comments and suggestions from the
public and affected agencies concerning
the proposed collection of information
are encouraged. Your comments should
address one or more of the following
four points:
—Evaluate whether the proposed
collection of information is necessary
for the proper performance of the
functions of the Bureau of Justice
Statistics, including whether the
information will have practical utility;
—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;
—Evaluate whether and if so how the
quality, utility, and clarity of the
information to be collected can be
enhanced; and
—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.
FOR FURTHER INFORMATION CONTACT:
jbell on DSKJLSW7X2PROD with NOTICES
Overview of This Information
Collection
1. Type of Information Collection:
Extension of a currently approved
collection.
2. The Title of the Form/Collection:
Federal Bureau of Investigation
Bioterrorism Preparedness Act: Entity/
Individual Information.
3. The agency form number, if any,
and the applicable component of the
Department sponsoring the collection:
The form is FD–961. The applicable
component within the Criminal Justice
Information Services Division,
Department of Justice (DOJ), Federal
Bureau of Investigation (FBI).
4. Affected public who will be asked
or required to respond, as well as a brief
abstract:.
Primary: City, country, state, federal,
individuals, business or other for profit,
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Jkt 253001
and not-for-profit institute. This
collection is needed to receive names
and other identifying information
submitted by individuals requesting
access to specific agents or toxins, and
consult with appropriate officials of the
Department of Health and Human
Services and the Department of
Agriculture as to whether certain
individuals specified in the provisions
should be denied access to or granted
limited access to specific agents.
5. An estimate of the total number of
respondents and the amount of time
estimated for an average respondent to
respond: There are approximately 3,655
(FY 2020) and respondents at 1 hour 30
minutes for the FD–961 form.
6. An estimate of the total public
burden (in hours) associated with the
collection: The estimated public burden
associated with this collection is
approximately 5,483 hours annual
burden, associated with this information
collection.
If additional information is required
contact: Melody Braswell, Department
Clearance Officer, United States
Department of Justice, Justice
Management Division, Policy and
Planning Staff, Two Constitution
Square, 145 N Street NE, 3E.405A,
Washington, DC 20530.
Dated: February 24, 2021.
Melody Braswell,
Department Clearance Officer for PRA, U.S.
Department of Justice.
[FR Doc. 2021–04208 Filed 3–1–21; 8:45 am]
BILLING CODE 4410–02–P
DEPARTMENT OF LABOR
Employee Benefits Security
Administration
State All Payer Claims Databases
Advisory Committee
Employee Benefits Security
Administration, Department of Labor.
ACTION: Notice.
AGENCY:
This notice announces the
establishment of the State All Payer
Claims Databases Advisory Committee
(Committee) and also solicits
nominations for members to be
appointed by the Secretary of Labor
(Secretary). The No Surprises Act,
enacted as part of the Consolidated
Appropriations Act, 2021, requires the
Department of Labor (DOL) to establish
(and periodically update) a standardized
reporting format for voluntary reporting
by group health plans to State All Payer
Claims Databases and provide guidance
to States on collecting data. The Act also
SUMMARY:
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directs the Secretary to convene an
advisory committee.
DATES: Nominations for membership
will be considered if they are received
by March 16, 2021.
ADDRESSES: Send nominations to
SAPCDACnominations@dol.gov to the
attention of Elizabeth Schumacher,
Office of Health Plan Standards and
Compliance Assistance, Employee
Benefits Security Administration, DOL.
FOR FURTHER INFORMATION CONTACT:
Elizabeth Schumacher, Employee
Benefits Security Administration, DOL
at 202–693–8335. For press inquiries
contact Grant Vaught, Office of Public
Affairs, DOL at 202–693–4672.
SUPPLEMENTARY INFORMATION:
I. Background
Section 735 of the Employee
Retirement Income Security Act of 1974,
as added by section 115(b) of the No
Surprises Act, enacted as part of the
Consolidated Appropriations Act, 2021,
div. BB, tit. I, Public Law 116–260 (Dec.
27, 2020), requires the DOL to establish
(and periodically update) a standardized
reporting format for voluntary reporting
by group health plans to State All Payer
Claims Databases and provide guidance
to States on collecting data. The Act also
directs the Secretary to convene an
advisory committee consisting of no
more than 15 members to advise the
Secretary regarding the format and
guidance for voluntary reporting by
group health plans to State All Payer
Claims Databases. The Committee will
remain in existence from the time of its
convention until it submits its report
with its recommendations to the
Secretary, the Committee on Health,
Education, Labor, and Pensions of the
Senate, and the Committee on Energy
and Commerce and the Committee on
Education and Labor of the House of
Representatives. The Committee is
governed by the provisions of the
Federal Advisory Committee Act, 5
U.S.C. App. 2.
II. Charter, General Responsibilities,
and Composition of the State All Payer
Claims Databases Advisory Committee
A. Charter Information and General
Responsibilities
On February 17, 2021, the Acting
Secretary approved the charter
establishing the Committee. The
Committee will advise the Secretary
regarding the standardized reporting
format for the voluntary reporting by
group health plans to State All Payer
Claims Databases. Reporting will
include medical claims, pharmacy
claims, dental claims, and eligibility
and provider files collected from private
E:\FR\FM\02MRN1.SGM
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]]>Agencies
[Federal Register Volume 86, Number 39 (Tuesday, March 2, 2021)]
[Notices]
[Pages 12207-12208]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2021-04208]
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DEPARTMENT OF JUSTICE
Federal Bureau of Investigation
[OMB Number 1110-0039]
Agency Information Collection Activities; Proposed eCollection
eComments Requested; Revision of a Currently Approved Collection
Bioterrorism Preparedness Act: Entity/Individual Information
AGENCY: Federal Bureau of Investigation, Criminal Justice Information
Services Division, Department of Justice.
ACTION: 60-Day notice.
-----------------------------------------------------------------------
SUMMARY: The Department of Justice (DOJ), Federal Bureau of
Investigation (FBI), Criminal Justice Information Services (CJIS)
Division will be submitting the following information collection
request to the Office of Management and Budget (OMB) for review and
approval in accordance with the Paperwork Reduction Act of 1995. The
proposed information collection is published to obtain comments from
the public and affected agencies.
DATES: Comments are encouraged and will be accepted for 60 days until
May 3, 2021.
[[Page 12208]]
FOR FURTHER INFORMATION CONTACT: If you have additional comments
especially on the estimated public burden or associated response time,
suggestions, or need a copy of the proposed information collection
instrument with instructions or additional information, please contact
James J. Sheets, Biometric Services Section, Identity Management Unit,
Federal Bureau of Investigation, CJIS Division, Biometric Technology
Center, 1000 Custer Hollow Road, Clarksburg, West Virginia 26306.
SUPPLEMENTARY INFORMATION: Written comments and suggestions from the
public and affected agencies concerning the proposed collection of
information are encouraged. Your comments should address one or more of
the following four points:
--Evaluate whether the proposed collection of information is necessary
for the proper performance of the functions of the Bureau of Justice
Statistics, including whether the information will have practical
utility;
--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;
--Evaluate whether and if so how the quality, utility, and clarity of
the information to be collected can be enhanced; and
--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.
Overview of This Information Collection
1. Type of Information Collection: Extension of a currently
approved collection.
2. The Title of the Form/Collection: Federal Bureau of
Investigation Bioterrorism Preparedness Act: Entity/Individual
Information.
3. The agency form number, if any, and the applicable component of
the Department sponsoring the collection: The form is FD-961. The
applicable component within the Criminal Justice Information Services
Division, Department of Justice (DOJ), Federal Bureau of Investigation
(FBI).
4. Affected public who will be asked or required to respond, as
well as a brief abstract:.
Primary: City, country, state, federal, individuals, business or
other for profit, and not-for-profit institute. This collection is
needed to receive names and other identifying information submitted by
individuals requesting access to specific agents or toxins, and consult
with appropriate officials of the Department of Health and Human
Services and the Department of Agriculture as to whether certain
individuals specified in the provisions should be denied access to or
granted limited access to specific agents.
5. An estimate of the total number of respondents and the amount of
time estimated for an average respondent to respond: There are
approximately 3,655 (FY 2020) and respondents at 1 hour 30 minutes for
the FD-961 form.
6. An estimate of the total public burden (in hours) associated
with the collection: The estimated public burden associated with this
collection is approximately 5,483 hours annual burden, associated with
this information collection.
If additional information is required contact: Melody Braswell,
Department Clearance Officer, United States Department of Justice,
Justice Management Division, Policy and Planning Staff, Two
Constitution Square, 145 N Street NE, 3E.405A, Washington, DC 20530.
Dated: February 24, 2021.
Melody Braswell,
Department Clearance Officer for PRA, U.S. Department of Justice.
[FR Doc. 2021-04208 Filed 3-1-21; 8:45 am]
BILLING CODE 4410-02-P
