Post-Marketing Pediatric-Focused Product Safety Reviews; Establishment of a Public Docket; Request for Comments, 9324-9325 [2018-04400]

Download as PDF 9324 Federal Register / Vol. 83, No. 43 / Monday, March 5, 2018 / Notices Estimated Total Annual Burden Hours: 2,925 hours. In compliance with the requirements of the Paperwork Reduction Act of 1995 (Pub. L. 104–13, 44 U.S.C. Chap 35), the Administration for Children and Families is soliciting public comment on the specific aspects of the information collection described above. Copies of the proposed collection of information can be obtained and comments may be forwarded by writing to the Administration for Children and Families, Office of Planning, Research and Evaluation, 330 C Street SW, Washington DC 20201. Attn: ACF Reports Clearance Officer. Email address: infocollection@acf.hhs.gov. All requests should be identified by the title of the information collection. The Department specifically requests comments on: (a) Whether the proposed collection of information is necessary for the proper performance of the functions of the agency, including whether the information shall have practical utility; (b) the accuracy of the agency’s estimate of the burden of the proposed collection of information; (c) the quality, utility, and clarity of the information to be collected; and (d) ways to minimize the burden of the collection of information on respondents, including through the use of automated collection techniques or other forms of information technology. Consideration will be given to comments and suggestions submitted within 60 days of this publication. Robert Sargis, Reports Clearance Officer. [FR Doc. 2018–04384 Filed 3–2–18; 8:45 am] BILLING CODE 4184–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration [Docket No. FDA–2017–N–7022] Post-Marketing Pediatric-Focused Product Safety Reviews; Establishment of a Public Docket; Request for Comments AGENCY: Food and Drug Administration, HHS. Notice, establishment of a public docket; request for comments. sradovich on DSK3GMQ082PROD with NOTICES ACTION: The Food and Drug Administration (FDA) is establishing a public docket to collect comments related to the post-marketing pediatricfocused safety reviews of products posted between October 23, 2017, and March 16, 2018, on FDA’s website but SUMMARY: VerDate Sep<11>2014 19:25 Mar 02, 2018 Jkt 244001 not presented at the March 23, 2018, Pediatric Advisory Committee (PAC) meeting. These reviews are intended to be available for review and comment by members of the PAC, interested parties (such as academic researchers, regulated industries, consortia, and patient groups), and the general public. DATES: Submit either electronic or written comments by March 30, 2018. ADDRESSES: FDA is establishing a docket for public comment on this document. The docket number is FDA–2017–N– 7022. The docket will close on March 30, 2018. Submit either electronic or written comments by that date. Please note that late, untimely comments will not be considered. Electronic comments must be submitted on or before March 30, 2018. The https:// www.regulations.gov electronic filing system will accept comments until midnight Eastern Time at the end of March 30, 2018. Comments received by mail/hand delivery/courier (for written/ paper submissions) will be considered timely if they are postmarked or the delivery service acceptance receipt is on or before that date. You may submit comments as follows: Electronic Submissions Submit electronic comments in the following way: • Federal eRulemaking Portal: https://www.regulations.gov. Follow the instructions for submitting comments. Comments submitted electronically, including attachments, to https:// www.regulations.gov will be posted to the docket unchanged. Because your comment will be made public, you are solely responsible for ensuring that your comment does not include any confidential information that you or a third party may not wish to be posted, such as medical information, your or anyone else’s Social Security number, or confidential business information, such as a manufacturing process. Please note that if you include your name, contact information, or other information that identifies you in the body of your comments, that information will be posted on https://www.regulations.gov. • If you want to submit a comment with confidential information that you do not wish to make available to the public, submit the comment as a written/paper submission and in the manner detailed (see ‘‘Written/Paper Submissions’’ and ‘‘Instructions’’). Written/Paper Submissions Submit written/paper submissions as follows: • Mail/Hand delivery/Courier (for written/paper submissions): Dockets PO 00000 Frm 00066 Fmt 4703 Sfmt 4703 Management Staff (HFA–305), Food and Drug Administration, 5630 Fishers Lane, Rm. 1061, Rockville, MD 20852. • For written/paper comments submitted to the Dockets Management Staff, FDA will post your comment, as well as any attachments, except for information submitted, marked and identified, as confidential, if submitted as detailed in ‘‘Instructions.’’ Instructions: All submissions received must include the Docket No. FDA– 2017–N–7022 for ‘‘Post-Marketing Pediatric-Focused Product Safety Reviews; Establishment of a Public Docket; Request for Comments.’’ Received comments, those filed in a timely manner (see ADDRESSES), will be placed in the docket and, except for those submitted as ‘‘Confidential Submissions,’’ publicly viewable at https://www.regulations.gov or at the Dockets Management Staff between 9 a.m. and 4 p.m., Monday through Friday. • Confidential Submissions—To submit a comment with confidential information that you do not wish to be made publicly available, submit your comments only as a written/paper submission. You should submit two copies total. One copy will include the information you claim to be confidential with a heading or cover note that states ‘‘THIS DOCUMENT CONTAINS CONFIDENTIAL INFORMATION.’’ FDA will review this copy, including the claimed confidential information, in its consideration of comments. The second copy, which will have the claimed confidential information redacted/ blacked out, will be available for public viewing and posted on https:// www.regulations.gov. Submit both copies to the Dockets Management Staff. If you do not wish your name and contact information to be made publicly available, you can provide this information on the cover sheet and not in the body of your comments and you must identify this information as ‘‘confidential.’’ Any information marked as ‘‘confidential’’ will not be disclosed except in accordance with 21 CFR 10.20 and other applicable disclosure law. For more information about FDA’s posting of comments to public dockets, see 80 FR 56469, September 18, 2015, or access the information at: https://www.gpo.gov/ fdsys/pkg/FR-2015-09-18/pdf/201523389.pdf. Docket: For access to the docket to read background documents or the electronic and written/paper comments received, go to https:// www.regulations.gov and insert the docket number, found in brackets in the heading of this document, into the ‘‘Search’’ box and follow the prompts E:\FR\FM\05MRN1.SGM 05MRN1 Federal Register / Vol. 83, No. 43 / Monday, March 5, 2018 / Notices and/or go to the Dockets Management Staff, 5630 Fishers Lane, Rm. 1061, Rockville, MD 20852. FOR FURTHER INFORMATION CONTACT: Kenneth Quinto, Office of the Commissioner, Food and Drug Administration, 10903 New Hampshire Ave., Bldg. 32, Rm. 5145, Silver Spring, MD 20993, 240–402–2221, kenneth.quinto@fda.hhs.gov. SUPPLEMENTARY INFORMATION: FDA is responsible for protecting the public health by assuring the safety, efficacy, and security of human and veterinary drugs, biological products, medical devices, our Nation’s food supply, cosmetics, and products that emit radiation. FDA is establishing a public docket, Docket No. FDA–2017–N–7022, to receive input on post-marketing pediatric-focused safety reviews of products posted between October 23, 2017, and March 16, 2018, available on FDA’s website at https://www.fda.gov/ AdvisoryCommittees/Committees MeetingMaterials/PediatricAdvisory Committee/ucm510701.htm but not presented at the March 23, 2018, PAC meeting. FDA welcomes comments by members of the PAC, as mandated by the Best Pharmaceuticals for Children Act (Pub. L. 107–109) and the Pediatric Research Equity Act of 2003 (Pub. L. 108–155), interested parties (such as academic researchers, regulated industries, consortia, and patient groups), and the general public. The docket number is FDA–2017–N–7022. The docket will open on March 19, 2018, and remain open until March 30, 2018. The post-marketing pediatricfocused safety reviews are for the following products from the following centers at FDA: Center for Biologics Evaluation and Research 1. EPICEL (cultured epidermal autographs) (humanitarian device exemption (HDE)) 2. GARDASIL 9 (Human Papillomavirus 9-valent Vaccine, Recombinant) 3. TRUMENBA (Meningococcal Group B Vaccine) sradovich on DSK3GMQ082PROD with NOTICES Center for Drug Evaluation and Research 1. ATROPINE SULFATE OPHTHALMIC SOLUTION, USP 1% 2. DYMISTA (azelastine hydrochloride/fluticasone propionate) 3. EDURANT (rilpivirine); COMPLERA (emtricitabine, rilpivirine, tenofovir disoproxil VerDate Sep<11>2014 19:25 Mar 02, 2018 Jkt 244001 fumarate); ODEFSEY (emtricitabine, rilpivirine, tenofovir alafenamide) 4. EMEND (aprepitant) capsule and oral suspension 5. EPIDUO FORTE (adapalene/ benzoyl peroxide, 0.3%/2.5%) gel 6. GADAVIST (gadobutrol); EOVIST (Primovist; gadoxetate disodium) 7. GENVOYA (elvitegravir, cobicistat, emtricitabine, and tenofovir alafenamide) oral tablets 8. KAPVAY (clonidine extendedrelease) tablets 9. MERREM IV (meropenem for injection) 10. NAFTIN (naftifine hydrochloride) 11. NUCALA (mepolizumab) 12. OTIPRIO (6% ciprofloxacin otic suspension) 13. PAZEO (olopatadine hydrochloride ophthalmic solution) 0.7% 14. QNASL (beclomethasone dipropionate) nasal aerosol 15. SAPHRIS (asenapine) 16. TIVICAY (dolutegravir) 17. TREXIMET (naproxen sodium; sumatriptan succinate) 18. VALCYTE (valganciclovir) Center for Devices and Radiological Health 1. FLOURISH PEDIATRIC ESOPHAGEAL ATRESIA DEVICE (HDE) Dated: February 28, 2018. Leslie Kux, Associate Commissioner for Policy. [FR Doc. 2018–04400 Filed 3–2–18; 8:45 am] BILLING CODE 4164–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES [Document Identifier OS–0990–New] Agency Information Collection Request; 60-Day Public Comment Request Office of the Secretary, HHS. Notice. AGENCY: ACTION: In compliance with the requirement of the Paperwork Reduction Act of 1995, the Office of the Secretary (OS), Department of Health and Human Services, is publishing the following summary of a proposed collection for public comment. DATES: Comments on the ICR must be received on or before May 4, 2018. ADDRESSES: Submit your comments to Sherrette.Funn@hhs.gov or by calling 202–795–7714. FOR FURTHER INFORMATION CONTACT: When submitting comments or requesting information, please include SUMMARY: PO 00000 Frm 00067 Fmt 4703 Sfmt 4703 9325 the document identifier 0990–New–60D and project title for reference to Sherrette.funn@hhs.gov or call the Reports Clearance Officer. SUPPLEMENTARY INFORMATION: Interested persons are invited to send comments regarding this burden estimate or any other aspect of this collection of information, including any of the following subjects: (1) The necessity and utility of the proposed information collection for the proper performance of the agency’s functions; (2) the accuracy of the estimated burden; (3) ways to enhance the quality, utility, and clarity of the information to be collected; and (4) the use of automated collection techniques or other forms of information technology to minimize the information collection burden. Title of the Collection: Trafficking Victim Assistance Program Social Network Analysis—Network Survey. Type of Collection: New. OMB No. 0990–NEW-Office of the Assistant Secretary for Planning and Evaluation–Administration for Children and Families’ Trafficking Victim Assistance Program Abstract The Office of the Assistant Secretary for Planning and Evaluation (ASPE), in partnership with the Administration for Children and Families (ACF), U.S. Department of Health and Human Services (HHS) is requesting Office of Management and Budget (OMB) approval for a new information collection request, ‘‘Trafficking Victim Assistance Program (TVAP) Network Survey.’’ ICF has been contracted to carry out this project under the guidance of ASPE and ACF. TVAP, as authorized by the Trafficking Victims Protection Act of 2000, provides comprehensive case management services to foreign-born victims of human trafficking residing in the United States. Since its inception, TVAP funding and infrastructure have remained relatively unchanged: Services are paid on a per capita basis, and funds are managed through three primary grantees that enter into cooperative agreements with service providers (subrecipients). Given the changing landscape and the greater understanding of the nature and extent of trafficking, HHS is undertaking a program assessment to understand whether any efficiencies can be gained in the program administration and structure. Building on an earlier fiscal year 2018 assessment to solicit qualitative feedback from a range of program stakeholders, the information collected for this program survey aims to help HHS determine if efficiencies can be E:\FR\FM\05MRN1.SGM 05MRN1

Agencies

[Federal Register Volume 83, Number 43 (Monday, March 5, 2018)]
[Notices]
[Pages 9324-9325]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2018-04400]


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

DEPARTMENT OF HEALTH AND HUMAN SERVICES

Food and Drug Administration

[Docket No. FDA-2017-N-7022]


Post-Marketing Pediatric-Focused Product Safety Reviews; 
Establishment of a Public Docket; Request for Comments

AGENCY: Food and Drug Administration, HHS.

ACTION: Notice, establishment of a public docket; request for comments.

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

SUMMARY: The Food and Drug Administration (FDA) is establishing a 
public docket to collect comments related to the post-marketing 
pediatric-focused safety reviews of products posted between October 23, 
2017, and March 16, 2018, on FDA's website but not presented at the 
March 23, 2018, Pediatric Advisory Committee (PAC) meeting. These 
reviews are intended to be available for review and comment by members 
of the PAC, interested parties (such as academic researchers, regulated 
industries, consortia, and patient groups), and the general public.

DATES: Submit either electronic or written comments by March 30, 2018.

ADDRESSES: FDA is establishing a docket for public comment on this 
document. The docket number is FDA-2017-N-7022. The docket will close 
on March 30, 2018. Submit either electronic or written comments by that 
date. Please note that late, untimely comments will not be considered. 
Electronic comments must be submitted on or before March 30, 2018. The 
https://www.regulations.gov electronic filing system will accept 
comments until midnight Eastern Time at the end of March 30, 2018. 
Comments received by mail/hand delivery/courier (for written/paper 
submissions) will be considered timely if they are postmarked or the 
delivery service acceptance receipt is on or before that date.
    You may submit comments as follows:

Electronic Submissions

    Submit electronic comments in the following way:
     Federal eRulemaking Portal: https://www.regulations.gov. 
Follow the instructions for submitting comments. Comments submitted 
electronically, including attachments, to https://www.regulations.gov 
will be posted to the docket unchanged. Because your comment will be 
made public, you are solely responsible for ensuring that your comment 
does not include any confidential information that you or a third party 
may not wish to be posted, such as medical information, your or anyone 
else's Social Security number, or confidential business information, 
such as a manufacturing process. Please note that if you include your 
name, contact information, or other information that identifies you in 
the body of your comments, that information will be posted on https://www.regulations.gov.
     If you want to submit a comment with confidential 
information that you do not wish to make available to the public, 
submit the comment as a written/paper submission and in the manner 
detailed (see ``Written/Paper Submissions'' and ``Instructions'').

Written/Paper Submissions

    Submit written/paper submissions as follows:
     Mail/Hand delivery/Courier (for written/paper 
submissions): Dockets Management Staff (HFA-305), Food and Drug 
Administration, 5630 Fishers Lane, Rm. 1061, Rockville, MD 20852.
     For written/paper comments submitted to the Dockets 
Management Staff, FDA will post your comment, as well as any 
attachments, except for information submitted, marked and identified, 
as confidential, if submitted as detailed in ``Instructions.''
    Instructions: All submissions received must include the Docket No. 
FDA-2017-N-7022 for ``Post-Marketing Pediatric-Focused Product Safety 
Reviews; Establishment of a Public Docket; Request for Comments.'' 
Received comments, those filed in a timely manner (see ADDRESSES), will 
be placed in the docket and, except for those submitted as 
``Confidential Submissions,'' publicly viewable at https://www.regulations.gov or at the Dockets Management Staff between 9 a.m. 
and 4 p.m., Monday through Friday.
     Confidential Submissions--To submit a comment with 
confidential information that you do not wish to be made publicly 
available, submit your comments only as a written/paper submission. You 
should submit two copies total. One copy will include the information 
you claim to be confidential with a heading or cover note that states 
``THIS DOCUMENT CONTAINS CONFIDENTIAL INFORMATION.'' FDA will review 
this copy, including the claimed confidential information, in its 
consideration of comments. The second copy, which will have the claimed 
confidential information redacted/blacked out, will be available for 
public viewing and posted on https://www.regulations.gov. Submit both 
copies to the Dockets Management Staff. If you do not wish your name 
and contact information to be made publicly available, you can provide 
this information on the cover sheet and not in the body of your 
comments and you must identify this information as ``confidential.'' 
Any information marked as ``confidential'' will not be disclosed except 
in accordance with 21 CFR 10.20 and other applicable disclosure law. 
For more information about FDA's posting of comments to public dockets, 
see 80 FR 56469, September 18, 2015, or access the information at: 
https://www.gpo.gov/fdsys/pkg/FR-2015-09-18/pdf/2015-23389.pdf.
    Docket: For access to the docket to read background documents or 
the electronic and written/paper comments received, go to https://www.regulations.gov and insert the docket number, found in brackets in 
the heading of this document, into the ``Search'' box and follow the 
prompts

[[Page 9325]]

and/or go to the Dockets Management Staff, 5630 Fishers Lane, Rm. 1061, 
Rockville, MD 20852.

FOR FURTHER INFORMATION CONTACT: Kenneth Quinto, Office of the 
Commissioner, Food and Drug Administration, 10903 New Hampshire Ave., 
Bldg. 32, Rm. 5145, Silver Spring, MD 20993, 240-402-2221, 
[email protected].

SUPPLEMENTARY INFORMATION: FDA is responsible for protecting the public 
health by assuring the safety, efficacy, and security of human and 
veterinary drugs, biological products, medical devices, our Nation's 
food supply, cosmetics, and products that emit radiation.
    FDA is establishing a public docket, Docket No. FDA-2017-N-7022, to 
receive input on post-marketing pediatric-focused safety reviews of 
products posted between October 23, 2017, and March 16, 2018, available 
on FDA's website at https://www.fda.gov/AdvisoryCommittees/CommitteesMeetingMaterials/PediatricAdvisoryCommittee/ucm510701.htm but 
not presented at the March 23, 2018, PAC meeting. FDA welcomes comments 
by members of the PAC, as mandated by the Best Pharmaceuticals for 
Children Act (Pub. L. 107-109) and the Pediatric Research Equity Act of 
2003 (Pub. L. 108-155), interested parties (such as academic 
researchers, regulated industries, consortia, and patient groups), and 
the general public. The docket number is FDA-2017-N-7022. The docket 
will open on March 19, 2018, and remain open until March 30, 2018. The 
post-marketing pediatric-focused safety reviews are for the following 
products from the following centers at FDA:

Center for Biologics Evaluation and Research

    1. EPICEL (cultured epidermal autographs) (humanitarian device 
exemption (HDE))
    2. GARDASIL 9 (Human Papillomavirus 9-valent Vaccine, Recombinant)
    3. TRUMENBA (Meningococcal Group B Vaccine)

Center for Drug Evaluation and Research

    1. ATROPINE SULFATE OPHTHALMIC SOLUTION, USP 1%
    2. DYMISTA (azelastine hydrochloride/fluticasone propionate)
    3. EDURANT (rilpivirine); COMPLERA (emtricitabine, rilpivirine, 
tenofovir disoproxil fumarate); ODEFSEY (emtricitabine, rilpivirine, 
tenofovir alafenamide)
    4. EMEND (aprepitant) capsule and oral suspension
    5. EPIDUO FORTE (adapalene/benzoyl peroxide, 0.3%/2.5%) gel
    6. GADAVIST (gadobutrol); EOVIST (Primovist; gadoxetate disodium)
    7. GENVOYA (elvitegravir, cobicistat, emtricitabine, and tenofovir 
alafenamide) oral tablets
    8. KAPVAY (clonidine extended-release) tablets
    9. MERREM IV (meropenem for injection)
    10. NAFTIN (naftifine hydrochloride)
    11. NUCALA (mepolizumab)
    12. OTIPRIO (6% ciprofloxacin otic suspension)
    13. PAZEO (olopatadine hydrochloride ophthalmic solution) 0.7%
    14. QNASL (beclomethasone dipropionate) nasal aerosol
    15. SAPHRIS (asenapine)
    16. TIVICAY (dolutegravir)
    17. TREXIMET (naproxen sodium; sumatriptan succinate)
    18. VALCYTE (valganciclovir)

Center for Devices and Radiological Health

    1. FLOURISH PEDIATRIC ESOPHAGEAL ATRESIA DEVICE (HDE)

    Dated: February 28, 2018.
Leslie Kux,
Associate Commissioner for Policy.
[FR Doc. 2018-04400 Filed 3-2-18; 8:45 am]
 BILLING CODE 4164-01-P
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