Performance Review Board Members, 58486-58487 [2015-24650]

Download as PDF 58486 Federal Register / Vol. 80, No. 188 / Tuesday, September 29, 2015 / Notices Expiration Date 01/31/2017). This Revision includes new requests for approval to: (1) Replace ‘‘Hepatitis C virus, past or present’’ and ‘‘Hepatitis C, acute’’ with ‘‘Hepatitis C’’ on the List of Nationally Notifiable Conditions, (2) replace all listed Arboviral conditions with an inclusive category, ‘‘Arboviral Diseases’’ on the List of Nationally Notifiable Conditions, (3) receive case notification data for Hantavirus infection, non-Hantavirus Pulmonary Syndrome, (4) receive case notification data for Acute Flaccid Myelitis should it become nationally notifiable, (5) receive case notification data for Amebic Encephalitis should it become nationally notifiable, (6) receive new laboratory and vaccine data elements for all conditions, and (7) receive new disease-specific data elements for Mumps, Pertussis, Varicella, Arboviral Diseases, and Sexually Transmitted Diseases (STD). Although this Revision includes case notifications that were not part of the last NNDSS Revision, the estimate of the average burden per response based on the burden tables from all of the consolidated applications has not Estimated Annualized Burden Hours Number of respondents Type of respondents Form name States .............................................................. Territories ........................................................ Cities ............................................................... Weekly and Annual ........................................ Weekly and Annual ........................................ Weekly and Annual ........................................ 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. 2015–24681 Filed 9–28–15; 8:45 am] BILLING CODE 4163–18–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Disease, Disability, and Injury Prevention and Control Special Emphasis Panel (SEP): Initial Review 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 a meeting for the initial review of applications in response to GH15–002: Conducting Public Health Research in Georgia, and GH16–002: Impact Evaluation of Combination HIV Prevention Intervention in Botswana under PEPFAR. TIME AND DATE: 9:30a.m.–1:30p.m., EST, November 4, 2015 (Closed). PLACE: Teleconference. STATUS: The meeting 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 Public Law 92– 463. VerDate Sep<11>2014 17:54 Sep 28, 2015 Jkt 235001 The meeting will include the initial review, discussion, and evaluation of applications received in response to GH15–002: Conducting Public Health Research in Georgia, and GH16–002: Impact Evaluation of Combination HIV Prevention Intervention in Botswana under PEPFAR. MATTERS FOR DISCUSSION: CONTACT PERSON FOR MORE INFORMATION: Centers for Disease Control and Prevention asabaliauskas on DSK5VPTVN1PROD with NOTICES changed. The burden on the states and cities is estimated to be 10 hours per response and the burden on the territories is estimated to be 5 hours per response. The addition of new vaccine, laboratory, and disease-specific data elements do not add any additional burden because the states, territories, and cities already collect those data elements. There will be no increase in burden for the states, territories, and cities to send those data elements to CDC. The estimated annual burden is 28,340 hours. Hylan Shoob, Scientific Review Officer, Center for Global Health (CGH) Science Office, CGH, CDC, 1600 Clifton Road NE., Mailstop D–69, Atlanta, Georgia 30033, Telephone: (404) 639–4796. 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 the Centers for Disease Control and Prevention and the Agency for Toxic Substances and Disease Registry. Claudette Grant, Acting Director, Management Analysis and Services Office, Centers for Disease Control and Prevention (CDC). [FR Doc. 2015–24657 Filed 9–28–15; 8:45 am] BILLING CODE 4163–18–P PO 00000 50 5 2 Number of responses per respondent 52 52 52 Fmt 4703 Sfmt 4703 10 5 10 DEPARTMENT OF HEALTH AND HUMAN SERVICES Centers for Disease Control and Prevention Performance Review Board Members Centers for Disease Control and Prevention (CDC), Department of Health and Human Services (HHS). ACTION: Notice. AGENCY: In this notice, the Centers for Disease Control and Prevention (CDC) located within the Department of Health and Human Services (HHS) is publishing the names of the Performance Review Board Members who are reviewing performance for Fiscal Year 2015. FOR FURTHER INFORMATION CONTACT: Sharon O’Brien, Deputy Director, Executive and Scientific Resources Office, Human Resources Office, Centers for Disease Control and Prevention, 4770 Buford Highway, Mailstop K–07, Atlanta, Georgia 30341, Telephone (770) 488–1781. SUPPLEMENTARY INFORMATION: Title 5, U.S.C. Section 4314(c)(4) of the Civil Service Reform Act of 1978, Public Law 95–454, requires that the appointment of Performance Review Board Members be published in the Federal Register. The following persons will serve on the CDC Performance Review Boards or Panels, which will oversee the evaluation of performance appraisals of Senior Executive Service members for the Fiscal Year 2015 review period: SUMMARY: Christine Branche, Co-Chair Frm 00025 Avg. burden per response (in hrs.) E:\FR\FM\29SEN1.SGM 29SEN1 58487 Federal Register / Vol. 80, No. 188 / Tuesday, September 29, 2015 / Notices James Seligman, Co-Chair Irma Arispe Janet Collins Hazel Dean Joseph Henderson Christine Kosmos Alan Kotch Jennifer Parker Judith Qualters Kalwant Smagh 202–395–7285, or emailed to oira_ submission@omb.eop.gov. All comments should be identified with the OMB control number 0910–0583. Also include the FDA docket number found in brackets in the heading of this document. FOR FURTHER INFORMATION CONTACT: FDA PRA Staff, Office of Operations, Food and Drug Administration, 8455 Colesville Rd., COLE–14526, Silver Spring, MD 20993–0002, PRAStaff@ fda.hhs.gov. SUPPLEMENTARY INFORMATION: In compliance with 44 U.S.C. 3507, FDA has submitted the following proposed collection of information to OMB for review and clearance. Dated: September 24, 2015. Veronica Kennedy, Acting Director, Division of the Executive Secretariat, Office of the Chief of Staff, Centers for Disease Control and Prevention. [FR Doc. 2015–24650 Filed 9–28–15; 8:45 am] BILLING CODE 4163–18–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration [Docket No. FDA–2012–N–0438] Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Early Food Safety Evaluation of New Non-Pesticidal Proteins Produced by New Plant Varieties Intended for Food Use AGENCY: Food and Drug Administration, HHS. ACTION: Notice. The Food and Drug Administration (FDA) is announcing that a proposed collection of information has been submitted to the Office of Management and Budget (OMB) for review and clearance under the Paperwork Reduction Act of 1995. DATES: Fax written comments on the collection of information by October 29, 2015. ADDRESSES: To ensure that comments on the information collection are received, OMB recommends that written comments be faxed to the Office of Information and Regulatory Affairs, OMB, Attn: FDA Desk Officer, FAX: SUMMARY: Early Food Safety Evaluation of New Non-Pesticidal Proteins Produced by New Plant Varieties Intended for Food Use OMB Control Number 0910–0583— Extension Since May 29, 1992, when we issued a policy statement on foods derived from new plant varieties, we have encouraged developers of new plant varieties, including those varieties that are developed through biotechnology, to consult with us early in the development process to discuss possible scientific and regulatory issues that might arise (57 FR 22984). The guidance entitled, ‘‘Recommendations for the Early Food Safety Evaluation of New Non-Pesticidal Proteins Produced by New Plant Varieties Intended for Food Use,’’ continues to foster early communication by encouraging developers to submit to us their evaluation of the food safety of their new protein. Such communication helps to ensure that any potential food safety issues regarding a new protein in a new plant variety are resolved early in development, prior to any possible inadvertent introduction into the food supply of the new protein. We believe that any food safety concern related to such material entering the food supply would be limited to the potential that a new protein in food from the plant variety could cause an allergic reaction in susceptible individuals or could be a toxin. The guidance describes the procedures for early food safety evaluation of new proteins produced by new plant varieties, including bioengineered food plants, and the procedures for communicating with us about the safety evaluation. Interested persons may use Form FDA 3666 to transmit their submission to the Office of Food Additive Safety in the Center for Food Safety and Applied Nutrition. Form FDA 3666 is entitled, ‘‘Early Food Safety Evaluation of a New Non-Pesticidal Protein Produced by a New Plant Variety (New Protein Consultation),’’ and may be used in lieu of a cover letter for a New Protein Consultation (NPC). Form FDA 3666 prompts a submitter to include certain elements of a NPC in a standard format and helps the respondent organize their submission to focus on the information needed for our safety review. The form, and elements that would be prepared as attachments to the form, may be submitted in electronic format via the Electronic Submission Gateway, or may be submitted in paper format, or as electronic files on physical media with paper signature page. The information is used by us to evaluate the food safety of a specific new protein produced by a new plant variety. In the Federal Register of June 19, 2015 (80 FR 35370), FDA published a 60-day notice requesting public comment on the proposed collection of information. No comments were received. Description of Respondents: The respondents to this collection of information are developers of new plant varieties intended for food use. We estimate the burden of this collection of information as follows: TABLE 1—ESTIMATED ANNUAL REPORTING BURDEN 1 Category FDA Form No. Number of responses per respondent Number of respondents Average burden per response Total annual responses Total hours asabaliauskas on DSK5VPTVN1PROD with NOTICES First four data components ...................... Two other data components .................... 3666 3666 6 6 1 1 6 6 4 16 24 96 Total .................................................. ........................ ........................ ........................ ........................ ........................ 120 1 There are no capital costs or operating and maintenance costs associated with this collection of information. The estimated number of annual responses and average burden per response are based on our experience VerDate Sep<11>2014 17:54 Sep 28, 2015 Jkt 235001 with early food safety evaluations. Completing an early food safety evaluation for a new protein from a new PO 00000 Frm 00026 Fmt 4703 Sfmt 4703 plant variety is a one-time burden (one evaluation per new protein). Many developers of novel plants may choose E:\FR\FM\29SEN1.SGM 29SEN1

Agencies

[Federal Register Volume 80, Number 188 (Tuesday, September 29, 2015)]
[Notices]
[Pages 58486-58487]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2015-24650]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Centers for Disease Control and Prevention


Performance Review Board Members

AGENCY: Centers for Disease Control and Prevention (CDC), Department of 
Health and Human Services (HHS).

ACTION: Notice.

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SUMMARY: In this notice, the Centers for Disease Control and Prevention 
(CDC) located within the Department of Health and Human Services (HHS) 
is publishing the names of the Performance Review Board Members who are 
reviewing performance for Fiscal Year 2015.

FOR FURTHER INFORMATION CONTACT: Sharon O'Brien, Deputy Director, 
Executive and Scientific Resources Office, Human Resources Office, 
Centers for Disease Control and Prevention, 4770 Buford Highway, 
Mailstop K-07, Atlanta, Georgia 30341, Telephone (770) 488-1781.

SUPPLEMENTARY INFORMATION: Title 5, U.S.C. Section 4314(c)(4) of the 
Civil Service Reform Act of 1978, Public Law 95-454, requires that the 
appointment of Performance Review Board Members be published in the 
Federal Register. The following persons will serve on the CDC 
Performance Review Boards or Panels, which will oversee the evaluation 
of performance appraisals of Senior Executive Service members for the 
Fiscal Year 2015 review period:

Christine Branche, Co-Chair

[[Page 58487]]

James Seligman, Co-Chair
Irma Arispe
Janet Collins
Hazel Dean
Joseph Henderson
Christine Kosmos
Alan Kotch
Jennifer Parker
Judith Qualters
Kalwant Smagh

    Dated: September 24, 2015.
Veronica Kennedy,
Acting Director, Division of the Executive Secretariat, Office of the 
Chief of Staff, Centers for Disease Control and Prevention.
[FR Doc. 2015-24650 Filed 9-28-15; 8:45 am]
 BILLING CODE 4163-18-P
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