Agency Forms Undergoing Paperwork Reduction Act Review, 13345-13346 [2013-04510]

Download as PDF 13345 Federal Register / Vol. 78, No. 39 / Wednesday, February 27, 2013 / Notices *Assumptions: One respondent per hospital, collection of data on median of 75 patients per hospital, average data collection time of 15 minutes per patient. Kimberly S. Lane, Deputy Director, Office of Scientific Integrity, Office of the Associate Director for Science, Office of the Director, Centers for Disease Control and Prevention. [FR Doc. 2013–04508 Filed 2–26–13; 8:45 am] BILLING CODE 4163–18–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Centers for Disease Control and Prevention [30Day–13–0263] Agency Forms Undergoing Paperwork Reduction Act Review The Centers for Disease Control and Prevention (CDC) publishes a list of information collection requests under review by the Office of Management and Budget (OMB) in compliance with the Paperwork Reduction Act (44 U.S.C. Chapter 35). To request a copy of these requests, call the CDC Reports Clearance Officer at (404) 639–5960 or send an email to omb@cdc.gov. Send written comments to CDC Desk Officer, Office of Management and Budget, Washington, DC 20503 or by fax to (202) 395–5806. Written comments should be received within 30 days of this notice. Proposed Project Requirements for the Importation of Nonhuman Primates into the United States (formerly Requirements for a Special Permit to Import Cynomolgus, African Green, or Rhesus Monkeys into the United States) (OMB Control No. 0920–0263 Exp.6/30/2014)—Revision— National Center Emerging and Zoonotic Infectious Diseases (NCEZID), Centers for Disease Control and Prevention (CDC). Background and Brief Description Since May 1990, CDC has monitored the arrival and/or uncrating of certain shipments of non-human primates imported into the United States under a special permit program specific to Cynomolgus, African Green, or Rhesus Monkeys. CDC has monitored compliance with this special permit through the collection of information focused on determining whether or not importers conduct adequate disease control practices. Importers were required to renew their special permit every 180 days. In February 2013, CDC promulgated two regulations pertaining to the importation of nonhuman primates. The first rule rule, Requirements for Importers of Nonhuman Primates (2/15/ 2013, Vol. 78, No. 32/p. 11522) 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. It also extended the time period for registration/permit renewal from 180 days to 2 years. The Special Permit has been withdrawn. The requirements found therein are now incorporated into the revised final rule for 42 CFR 71.53. The second rule, Establishment of User Fees for Filovirus Testing of Nonhuman Primate Liver Samples (2/12/2013, Vol.78, No. 29, p.9828), outlines a process by which importers can send liver tissues to CDC from primates that die during importation from reasons other than trauma. CDC performs these tests due to the absence of a private sector option. CDC feels these regulatory changes balance the public health risks posed by the importation of nonhuman primates with the burden imposed on regulating their importation. These rule changes have prompted CDC to modify how it administers the information collected from the public in the enforcement of nonhuman primate regulations. CDC is requesting the following changes: 1. CDC requests that this information collection request be re-named ‘‘Requirements for the Importation of Nonhuman Primates into the United States’’ to more accurately reflect the type of information that is requested from respondents. 2. To streamline administration of this information collection request, CDC requests that CDC form 75.10A Application for Registration as an Importer of Nonhuman Primates and the Recordkeeping requirement currently approved under OMB Control Number 0920–0134 Foreign Quarantine Regulations, be moved and included in this revision to OMB Control Number 0920–0263. This action places all nonhuman primate information collection requirements and requests into one information collection request administered by CDC. 3. CDC is renaming the different portions of the information collected in this information collection to more accurately list the types of forms and documentation CDC collects from importers of nonhuman primates. Therefore, the former information categories of Businesses (limited permit), Businesses (extended permit), and Organizations (extended permit) are being renamed and reorganized. The information contained in these categories will now be accounted for in the Documentation sections of the burden table. This categorization will more accurately reflect CDC’s interaction with the importers. 4. CDC also requests additional burden hours to account for notification to CDC from importers of shipment arrivals and requests for release from quarantine. 5. CDC further requests the addition of the Filovirus Diagnostic Specimen Submission Form for Non-human Primate Materials, which will be used to collect all of the necessary information from nonhuman primate importers to test nonhuman primate liver samples for filovirus and communicate the results of this test. This action adds approximately 50 hours of burden to this information collection request. This information collection involves minimal personally identifiable information and should have limited impact on an individual’s privacy. There are no costs to respondents other than their time. The total burden requested for this information collection is 146. erowe on DSK2VPTVN1PROD with NOTICES ESTIMATED ANNUALIZED BURDEN HOURS Type of respondent Nonhuman Primate Importer .......................... Nonhuman Primate Importer .......................... VerDate Mar<15>2010 15:18 Feb 26, 2013 Jkt 229001 71.53(g) New Importer Nonhuman Primates. 71.53(g) Importer ReNonhuman Primates. PO 00000 Frm 00046 Fmt 4703 Number of responses per respondent Number of respondents Form name/CFR reference Average burden per response (in hours) Registration— 1 1 10/60 Registration— 12 1 10/60 Sfmt 4703 E:\FR\FM\27FEN1.SGM 27FEN1 13346 Federal Register / Vol. 78, No. 39 / Wednesday, February 27, 2013 / Notices ESTIMATED ANNUALIZED BURDEN HOURS—Continued Form name/CFR reference Nonhuman Primate Importer .......................... 71.53(h) Documentation (no form) (New Importer). 71.53(h) Documentation (no form) (Registered Importer). Recordkeeping and reporting requirements for importing NHPs: Notification of shipment arrival 71.53(n) (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 .......................... Kimberly S. Lane, Deputy Director, Office of Scientific Integrity, Office of the Associate Director for Science, Office of the Director, Centers for Disease Control and Prevention. [FR Doc. 2013–04510 Filed 2–26–13; 8:45 am] BILLING CODE 4163–18–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Centers for Medicare & Medicaid Services Medicare Program; Changes to the Semi-Annual Meeting of the Advisory Panel on Hospital Outpatient Payment (HOP Panel)—March 11 and March 12, 2013 Centers for Medicare & Medicaid Services (CMS), HHS. ACTION: Notice of meeting date and time, location, and format change. AGENCY: SUMMARY: This notice announces changes to the meeting date and time, location, and format of the first semiannual public meeting of 2013 that was announced and published in the Federal Register on November 26, 2012, entitled ‘‘Medicare Program; SemiAnnual Meeting of the Advisory Panel on Hospital Outpatient Payment (HOP Panel)—March 11 and 12, 2013.’’ DATES: Monday, March 11, 2013, from 1 p.m. to 5 p.m. Eastern Daylight Time (EDT). FOR FURTHER INFORMATION CONTACT: erowe on DSK2VPTVN1PROD with NOTICES Chuck Braver, (410) 786–3985. SUPPLEMENTARY INFORMATION: I. Background On November 26, 2012, we published a notice in the Federal Register (77 FR 70447) announcing the first semi-annual meeting of the Advisory Panel on VerDate Mar<15>2010 15:18 Feb 26, 2013 Jkt 229001 Hospital Outpatient Payment (HOP, the Panel) for 2013. We note that the November 26, 2012 notice provides specific information on the purpose of the meeting and the agenda. This information remains the same and has not changed with the exception of the meeting date and time, location, and format as specified in this notice. We refer readers to that previously published notice for general information. II. Provisions of the Notice [CMS–1597–N2] The November 26, 2012, notice announced an in-person meeting to be held over two days, March 11 through 12, 2013. Since the publication of that notice, the date and time, location, and format of the Panel meeting has changed. Therefore, we are publishing this notice to provide the public with the necessary information related to this upcoming public Panel meeting. First, the November 26, 2012, notice included the published date of the Panel meeting as Monday, March 11, 2013, from 1 p.m. to 5 p.m. EDT and Tuesday, March 12, 2013, from 9 a.m. to 5 p.m. EDT. The Panel meeting date and time has been changed and will only take place on March 11, 2013, from 1 p.m. to 5 p.m. EDT. Second, the November 26, 2012 notice included, the published meeting location as the CMS Central Office Auditorium, 7500 Security Boulevard, Woodlawn, Maryland 21244–1850. The Panel meeting format has been changed to Teleconference, Webcast, and Webinar. Therefore, there will no longer be an in-person meeting location for this public Panel meeting. Participants should view the CMS Web site at: http://cms.hhs.gov/Regulations-andGuidance/Guidance/FACA/Advisory PanelonAmbulatoryPayment ClassificationGroups.html for the most current details regarding the meeting. PO 00000 Frm 00047 Fmt 4703 Sfmt 9990 Number of responses per respondent Number of respondents Type of respondent Average burden per response (in hours) 1 1 10 12 1 30/60 25 6 15/60 25 10 6 15 15/60 20/60 Participants who have registered to attend the in-person meeting based on the November 26, 2012 notice do not have to re-register. The teleconference dial-in instructions, and related webcast and webinar details will be posted on the CMS Web site approximately 1 week prior to the meeting at: http:// cms.hhs.gov/Regulations-andGuidance/Guidance/FACA/ AdvisoryPanelonAmbulatoryPayment ClassificationGroups.html. Interested participants who did not register will be able to access the teleconference, webcast, and webinar by following the instructions on the above CMS Web site. III. Collection of Information Requirements This document does not impose information collection and recordkeeping requirements. Consequently, it need not be reviewed by the Office of Management and Budget under the authority of the Paperwork Reduction Act of 1995 (44 U.S.C. 35). (Catalog of Federal Domestic Assistance Program; No. 93.773 Medicare—Hospital Insurance Program; and No. 93.774, Medicare—Supplementary Medical Insurance Program) Dated: February 20, 2012. Marilyn Tavenner, Acting Administrator, Centers for Medicare & Medicaid Services. [FR Doc. 2013–04524 Filed 2–22–13; 4:15 pm] BILLING CODE 4120–01–P E:\FR\FM\27FEN1.SGM 27FEN1

Agencies

[Federal Register Volume 78, Number 39 (Wednesday, February 27, 2013)]
[Notices]
[Pages 13345-13346]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2013-04510]


-----------------------------------------------------------------------

DEPARTMENT OF HEALTH AND HUMAN SERVICES

Centers for Disease Control and Prevention

[30Day-13-0263]


Agency Forms Undergoing Paperwork Reduction Act Review

    The Centers for Disease Control and Prevention (CDC) publishes a 
list of information collection requests under review by the Office of 
Management and Budget (OMB) in compliance with the Paperwork Reduction 
Act (44 U.S.C. Chapter 35). To request a copy of these requests, call 
the CDC Reports Clearance Officer at (404) 639-5960 or send an email to 
omb@cdc.gov. Send written comments to CDC Desk Officer, Office of 
Management and Budget, Washington, DC 20503 or by fax to (202) 395-
5806. Written comments should be received within 30 days of this 
notice.

Proposed Project

    Requirements for the Importation of Nonhuman Primates into the 
United States (formerly Requirements for a Special Permit to Import 
Cynomolgus, African Green, or Rhesus Monkeys into the United States) 
(OMB Control No. 0920-0263 Exp.6/30/2014)--Revision--National Center 
Emerging and Zoonotic Infectious Diseases (NCEZID), Centers for Disease 
Control and Prevention (CDC).

Background and Brief Description

    Since May 1990, CDC has monitored the arrival and/or uncrating of 
certain shipments of non-human primates imported into the United States 
under a special permit program specific to Cynomolgus, African Green, 
or Rhesus Monkeys. CDC has monitored compliance with this special 
permit through the collection of information focused on determining 
whether or not importers conduct adequate disease control practices. 
Importers were required to renew their special permit every 180 days.
    In February 2013, CDC promulgated two regulations pertaining to the 
importation of nonhuman primates. The first rule rule, Requirements for 
Importers of Nonhuman Primates (2/15/2013, Vol. 78, No. 32/p. 11522) 
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. It 
also extended the time period for registration/permit renewal from 180 
days to 2 years. The Special Permit has been withdrawn. The 
requirements found therein are now incorporated into the revised final 
rule for 42 CFR 71.53. The second rule, Establishment of User Fees for 
Filovirus Testing of Nonhuman Primate Liver Samples (2/12/2013, Vol.78, 
No. 29, p.9828), outlines a process by which importers can send liver 
tissues to CDC from primates that die during importation from reasons 
other than trauma. CDC performs these tests due to the absence of a 
private sector option. CDC feels these regulatory changes balance the 
public health risks posed by the importation of nonhuman primates with 
the burden imposed on regulating their importation.
    These rule changes have prompted CDC to modify how it administers 
the information collected from the public in the enforcement of 
nonhuman primate regulations. CDC is requesting the following changes:
    1. CDC requests that this information collection request be re-
named ``Requirements for the Importation of Nonhuman Primates into the 
United States'' to more accurately reflect the type of information that 
is requested from respondents.
    2. To streamline administration of this information collection 
request, CDC requests that CDC form 75.10A Application for Registration 
as an Importer of Nonhuman Primates and the Recordkeeping requirement 
currently approved under OMB Control Number 0920-0134 Foreign 
Quarantine Regulations, be moved and included in this revision to OMB 
Control Number 0920-0263. This action places all nonhuman primate 
information collection requirements and requests into one information 
collection request administered by CDC.
    3. CDC is renaming the different portions of the information 
collected in this information collection to more accurately list the 
types of forms and documentation CDC collects from importers of 
nonhuman primates. Therefore, the former information categories of 
Businesses (limited permit), Businesses (extended permit), and 
Organizations (extended permit) are being renamed and reorganized. The 
information contained in these categories will now be accounted for in 
the Documentation sections of the burden table. This categorization 
will more accurately reflect CDC's interaction with the importers.
    4. CDC also requests additional burden hours to account for 
notification to CDC from importers of shipment arrivals and requests 
for release from quarantine.
    5. CDC further requests the addition of the Filovirus Diagnostic 
Specimen Submission Form for Non-human Primate Materials, which will be 
used to collect all of the necessary information from nonhuman primate 
importers to test nonhuman primate liver samples for filovirus and 
communicate the results of this test. This action adds approximately 50 
hours of burden to this information collection request.
    This information collection involves minimal personally 
identifiable information and should have limited impact on an 
individual's privacy. There are no costs to respondents other than 
their time.
    The total burden requested for this information collection is 146.

                                        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.............  71.53(g) New Importer                  1               1           10/60
                                         Registration--Nonhuman
                                         Primates.
Nonhuman Primate Importer.............  71.53(g) Importer Re-                 12               1           10/60
                                         Registration--Nonhuman
                                         Primates.

[[Page 13346]]

 
Nonhuman Primate Importer.............  71.53(h) Documentation                 1               1              10
                                         (no form) (New
                                         Importer).
Nonhuman Primate Importer.............  71.53(h) Documentation                12               1           30/60
                                         (no form) (Registered
                                         Importer).
Nonhuman Primate Importer.............  Recordkeeping and                     25               6           15/60
                                         reporting requirements
                                         for importing NHPs:
                                         Notification of
                                         shipment arrival
                                         71.53(n) (no form).
Nonhuman Primate Importer.............  Quarantine release                    25               6           15/60
                                         71.53(l) (No form).
Nonhuman Primate Importer.............  71.53 (v)...............              10              15           20/60
                                        Form: Filovirus
                                         Diagnostic Specimen
                                         Submission Form for Non-
                                         human Primate Materials.
----------------------------------------------------------------------------------------------------------------


Kimberly S. Lane,
Deputy Director, Office of Scientific Integrity, Office of the 
Associate Director for Science, Office of the Director, Centers for 
Disease Control and Prevention.
[FR Doc. 2013-04510 Filed 2-26-13; 8:45 am]
BILLING CODE 4163-18-P