83 FR 10484 - Agency Forms Undergoing Paperwork Reduction Act Review
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention Federal Register Volume 83, Issue 47 (March 9, 2018)
Centers for Disease Control and Prevention
Federal Register Volume 83, Issue 47 (March 9, 2018)
| Page Range | 10484-10485 | |
| FR Document | 2018-04742 |
[Federal Register Volume 83, Number 47 (Friday, March 9, 2018)] [Notices] [Pages 10484-10485] From the Federal Register Online [www.thefederalregister.org] [FR Doc No: 2018-04742] ======================================================================= ----------------------------------------------------------------------- DEPARTMENT OF HEALTH AND HUMAN SERVICES Centers for Disease Control and Prevention [30Day-18-0199] 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 Application for Permit to Import Biological Agents and Vectors of Human Disease into the United States and Application for Permit to Import or Transport Live Bats (42 CFR 71.54) 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 September 26, 2017 to obtain comments from the public and affected agencies. CDC received three 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 or send an email to [email protected]. 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 Import Permit Applications (42 CFR 71.54) (OMB Control Number 0920- 0199, expires 12/31/2019)--Revision--Office of Public Health Preparedness and Response (OPHPR), Centers for Disease Control and Prevention (CDC). Background and Brief Description On September 26, 2017, CDC published a 60-day Federal Register notice (82 FR 44795) seeking public comments to initiate a revision of the information collection projects titled ``Application for Permit to Import Biological Agents, Infectious Substances and Vectors of Human Disease into the United States'' and ``Application for Permit to Import or Transport Live Bats.'' As a result of this notice, CDC received three comments. One commenter requested that we make the ``Application for Permit to Import [[Page 10485]] Biological Agents, Infectious Substances and Vectors of Human Disease into the United States'' form fillable so that applicants are able to complete the electronically. We made no changes based on this comment but note that the form will be published as a pdf-fillable form so that applicants have the ability to save the document to the applicant's local drive, complete the form, and then mail or fax the application to CDC. The other two comments did not pertain to the changes to the forms. Therefore, we made no changes to forms based on these comments. The Application for Permit to Import Biological Agents, Infectious Substances and Vectors of Human Disease into the United States form is used by laboratory facilities, such as those operated by government agencies, universities, and research institutions to request a permit for the importation of biological agents, infectious substances, or vectors of human disease. This form has been revised to remove questions that are duplicative or not required to process the import permit request and added questions requesting biosafety officer's contact information and verifying biosafety measures for any subsequent transfers listed on the import permit application of infectious biological agent, infectious substance, and/or vector once in the United States. The Application for Permit to Import or Transport Live Bats form is used by laboratory facilities such as those operated by government agencies, universities, research institutions, and for educational, exhibition or scientific purposes to request a permit for the importation, and any subsequent distribution after importation, of live bats. This form currently requests the applicant and sender contact information; a description and intended use of bats to be imported; and facility isolation and containment information. CDC revised this application to add a question about what personal protective measures will be used. Estimates of burden for the survey are based on information obtained from the CDC import permit database on the number of permits issued on annual basis since 2010. CDC estimates 1,322 burden hours for this collection. Estimated Annualized Burden Hours ---------------------------------------------------------------------------------------------------------------- Number of Average burden Type of respondent Form name Number of responses per per response respondents respondent (in hours) ---------------------------------------------------------------------------------------------------------------- Applicants Requesting to Import Application for Permit to 2,000 1 20/60 Biological Agents, Infectious Import Biological Agents, Substances and Vectors. Infectious Substances and Vectors of Human Disease into the United States. Applicants Requesting to Import Application for Permit to 2,000 1 10/60 Biological Agents, Infectious Import Biological Agents, Substances and Vectors. Infectious Substances and Vectors of Human Disease into the United States Guidance. Applicants Requesting to Import Application for Permit to 380 1 50/60 Biological Agents, Infectious Import Biological Agents, Substances and Vectors. Infectious Substances and Vectors of Human Disease into the United States- Subsequent Transfer. Applicants Requesting to Import Application for a Permit to 10 1 20/60 Live Bats. Import Live Bats. Applicants Requesting to Import Application for a Permit to 10 1 10/60 Live Bats. Import Live Bats Guidance. ---------------------------------------------------------------------------------------------------------------- Leroy A. Richardson, Chief, Information Collection Review Office, Office of Scientific Integrity, Office of the Associate Director for Science, Office of the Director, Centers for Disease Control and Prevention. [FR Doc. 2018-04742 Filed 3-8-18; 8:45 am] BILLING CODE 4163-18-P
![10484 Federal Register / Vol. 83, No. 47 / Friday, March 9, 2018 / Notices
public-comments. Postal mail addressed the comment must include the factual to allow an additional 30 days for public
to the Commission is subject to delay and legal basis for the request, and must and affected agency comments.
due to heightened security screening. As identify the specific portions of the CDC will accept all comments for this
a result, we encourage you to submit comment to be withheld from the public proposed information collection project.
your comments online. To make sure record. See FTC Rule 4.9(c). Your The Office of Management and Budget
that the Commission considers your comment will be kept confidential only is particularly interested in comments
online comment, you must file it at if the General Counsel grants your that:
https://ftcpublic.commentworks.com/ request in accordance with the law and (a) Evaluate whether the proposed
ftc/furrulespra1 by following the the public interest. Once your comment collection of information is necessary
instructions on the web based form. If has been posted on the public FTC for the proper performance of the
this Notice appears at https:// website—as legally required by FTC functions of the agency, including
www.regulations.gov, you also may file Rule 4.9(b)—we cannot redact or whether the information will have
a comment through that website. remove your comment from the FTC practical utility;
If you file your comment on paper, website, unless you submit a (b) Evaluate the accuracy of the
write ‘‘Paperwork Reduction Act: FTC confidentiality request that meets the agencies estimate of the burden of the
File No. P072108’’ on your comment requirements for such treatment under proposed collection of information,
and on the envelope, and mail your FTC Rule 4.9(c), and the General including the validity of the
comment to the following address: Counsel grants that request. methodology and assumptions used;
Federal Trade Commission, Office of the Visit the Commission website at (c) Enhance the quality, utility, and
Secretary, 600 Pennsylvania Avenue https://www.ftc.gov to read this Notice. clarity of the information to be
NW, Suite CC–5610 (Annex C), The FTC Act and other laws that the collected;
Washington, DC 20580, or deliver your Commission administers permit the (d) Minimize the burden of the
comment to the following address: collection of public comments to collection of information on those who
Federal Trade Commission, Office of the consider and use in this proceeding as are to respond, including, through the
Secretary, Constitution Center, 400 7th appropriate. The Commission will use of appropriate automated,
Street SW, 5th Floor, Suite 5610, consider all timely and responsive electronic, mechanical, or other
Washington, DC 20024. If possible, public comments that it receives on or technological collection techniques or
submit your paper comment to the before May 8, 2018. You can find more other forms of information technology,
Commission by courier or overnight information, including routine uses e.g., permitting electronic submission of
service. permitted by the Privacy Act, in the responses; and
Because your comment will be placed Commission’s privacy policy, at https:// (e) Assess information collection
on the publicly accessible FTC website www.ftc.gov/site-information/privacy- costs.
at https://www.ftc.gov, you are solely policy. To request additional information on
responsible for making sure that your the proposed project or to obtain a copy
comment does not include any sensitive David C. Shonka, of the information collection plan and
or confidential information. In Acting General Counsel. instruments, call (404) 639–7570 or
particular, your comment should not [FR Doc. 2018–04825 Filed 3–8–18; 8:45 am] send an email to omb@cdc.gov. Direct
include any sensitive personal BILLING CODE 6750–01–P written comments and/or suggestions
information, such as your or anyone regarding the items contained in this
else’s Social Security number; date of notice to the Attention: CDC Desk
birth; driver’s license number or other DEPARTMENT OF HEALTH AND Officer, Office of Management and
state identification number, or foreign HUMAN SERVICES Budget, 725 17th Street NW,
country equivalent; passport number; Washington, DC 20503 or by fax to (202)
financial account number; or credit or Centers for Disease Control and 395–5806. Provide written comments
debit card number. You are also solely Prevention within 30 days of notice publication.
responsible for making sure that your
[30Day–18–0199] Proposed Project
comment does not include any sensitive
health information, such as medical Agency Forms Undergoing Paperwork Import Permit Applications (42 CFR
records or other individually Reduction Act Review 71.54) (OMB Control Number 0920–
identifiable health information. In 0199, expires 12/31/2019)—Revision—
addition, your comment should not In accordance with the Paperwork Office of Public Health Preparedness
include any ‘‘trade secret or any Reduction Act of 1995, the Centers for and Response (OPHPR), Centers for
commercial or financial information Disease Control and Prevention (CDC) Disease Control and Prevention (CDC).
which . . . is privileged or has submitted the information
collection request titled Application for Background and Brief Description
confidential’’—as provided by Section
6(f) of the FTC Act, 15 U.S.C. 46(f), and Permit to Import Biological Agents and On September 26, 2017, CDC
FTC Rule 4.10(a)(2), 16 CFR 4.10(a)(2)— Vectors of Human Disease into the published a 60-day Federal Register
including in particular competitively United States and Application for notice (82 FR 44795) seeking public
sensitive information such as costs, Permit to Import or Transport Live Bats comments to initiate a revision of the
sales statistics, inventories, formulas, (42 CFR 71.54) to the Office of information collection projects titled
patterns, devices, manufacturing Management and Budget (OMB) for ‘‘Application for Permit to Import
processes, or customer names. review and approval. CDC previously Biological Agents, Infectious Substances
amozie on DSK30RV082PROD with NOTICES
Comments containing material for published a ‘‘Proposed Data Collection and Vectors of Human Disease into the
which confidential treatment is Submitted for Public Comment and United States’’ and ‘‘Application for
requested must be filed in paper form, Recommendations’’ notice on Permit to Import or Transport Live
must be clearly labeled ‘‘Confidential,’’ September 26, 2017 to obtain comments Bats.’’ As a result of this notice, CDC
and must comply with FTC Rule 4.9(c). from the public and affected agencies. received three comments. One
In particular, the written request for CDC received three comments related to commenter requested that we make the
confidential treatment that accompanies the previous notice. This notice serves ‘‘Application for Permit to Import
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![Federal Register / Vol. 83, No. 47 / Friday, March 9, 2018 / Notices 10485
Biological Agents, Infectious Substances government agencies, universities, and for educational, exhibition or scientific
and Vectors of Human Disease into the research institutions to request a permit purposes to request a permit for the
United States’’ form fillable so that for the importation of biological agents, importation, and any subsequent
applicants are able to complete the infectious substances, or vectors of distribution after importation, of live
electronically. We made no changes human disease. This form has been bats. This form currently requests the
based on this comment but note that the revised to remove questions that are applicant and sender contact
form will be published as a pdf-fillable duplicative or not required to process information; a description and intended
form so that applicants have the ability the import permit request and added use of bats to be imported; and facility
to save the document to the applicant’s questions requesting biosafety officer’s isolation and containment information.
local drive, complete the form, and then contact information and verifying
CDC revised this application to add a
mail or fax the application to CDC. The biosafety measures for any subsequent
question about what personal protective
other two comments did not pertain to transfers listed on the import permit
the changes to the forms. Therefore, we application of infectious biological measures will be used.
made no changes to forms based on agent, infectious substance, and/or Estimates of burden for the survey are
these comments. vector once in the United States. based on information obtained from the
The Application for Permit to Import The Application for Permit to Import CDC import permit database on the
Biological Agents, Infectious Substances or Transport Live Bats form is used by number of permits issued on annual
and Vectors of Human Disease into the laboratory facilities such as those basis since 2010. CDC estimates 1,322
United States form is used by laboratory operated by government agencies, burden hours for this collection.
facilities, such as those operated by universities, research institutions, and
ESTIMATED ANNUALIZED BURDEN HOURS
Average
Number of
Number of burden per
Type of respondent Form name responses per
respondents response
respondent (in hours)
Applicants Requesting to Import Biological Application for Permit to Import Biological 2,000 1 20/60
Agents, Infectious Substances and Vectors. Agents, Infectious Substances and Vectors
of Human Disease into the United States.
Applicants Requesting to Import Biological Application for Permit to Import Biological 2,000 1 10/60
Agents, Infectious Substances and Vectors. Agents, Infectious Substances and Vectors
of Human Disease into the United States
Guidance.
Applicants Requesting to Import Biological Application for Permit to Import Biological 380 1 50/60
Agents, Infectious Substances and Vectors. Agents, Infectious Substances and Vectors
of Human Disease into the United States-
Subsequent Transfer.
Applicants Requesting to Import Live Bats .... Application for a Permit to Import Live Bats .. 10 1 20/60
Applicants Requesting to Import Live Bats .... Application for a Permit to Import Live Bats 10 1 10/60
Guidance.
Leroy A. Richardson, (OMB) for review and approval. CDC (c) Enhance the quality, utility, and
Chief, Information Collection Review Office, previously published a ‘‘Proposed Data clarity of the information to be
Office of Scientific Integrity, Office of the Collection Submitted for Public collected;
Associate Director for Science, Office of the Comment and Recommendations’’ (d) Minimize the burden of the
Director, Centers for Disease Control and notice on December 21, 2017 to obtain collection of information on those who
Prevention. comments from the public and affected are to respond, including, through the
[FR Doc. 2018–04742 Filed 3–8–18; 8:45 am] agencies. CDC did not receive comments use of appropriate automated,
BILLING CODE 4163–18–P related to the previous notice. This electronic, mechanical, or other
notice serves to allow an additional 30 technological collection techniques or
days for public and affected agency other forms of information technology,
DEPARTMENT OF HEALTH AND comments. e.g., permitting electronic submission of
HUMAN SERVICES CDC will accept all comments for this responses; and
proposed information collection project. (e) Assess information collection
Centers for Disease Control and The Office of Management and Budget costs.
Prevention is particularly interested in comments To request additional information on
that: the proposed project or to obtain a copy
[30Day–18–18EV]
(a) Evaluate whether the proposed of the information collection plan and
Agency Forms Undergoing Paperwork collection of information is necessary instruments, call (404) 639–7570 or
Reduction Act Review for the proper performance of the send an email to omb@cdc.gov. Direct
functions of the agency, including written comments and/or suggestions
amozie on DSK30RV082PROD with NOTICES
In accordance with the Paperwork whether the information will have regarding the items contained in this
Reduction Act of 1995, the Centers for practical utility; notice to the Attention: CDC Desk
Disease Control and Prevention (CDC) (b) Evaluate the accuracy of the Officer, Office of Management and
has submitted the information agencies estimate of the burden of the Budget, 725 17th Street NW,
collection request titled Enhanced proposed collection of information, Washington, DC 20503 or by fax to (202)
Surveillance for Histoplasmosis to the including the validity of the 395–5806. Provide written comments
Office of Management and Budget methodology and assumptions used; within 30 days of notice publication.
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Document Created: 2018-03-09 03:48:18
Document Modified: 2018-03-09 03:48:18
| Category | Regulatory Information | |
| Collection | Federal Register | |
| sudoc Class | AE 2.7: GS 4.107: AE 2.106: | |
| Publisher | Office of the Federal Register, National Archives and Records Administration | |
| Section | Notices | |
| FR Citation | 83 FR 10484 |
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