Antiseptic Patient Preoperative Skin Preparation Products; Public Hearing; Request for Comments; Correction, 71804 [2012-29166]

Download as PDF 71804 Federal Register / Vol. 77, No. 233 / Tuesday, December 4, 2012 / Notices and 4 p.m., Monday through Friday, and will be posted to the docket at https:// www.regulations.gov. III. Paperwork Reduction Act of 1995 This guidance refers to previously approved collections of information found in FDA regulations. These collections of information are subject to review by the Office of Management and Budget (OMB) under the Paperwork Reduction Act of 1995 (44 U.S.C. 3501– 3520). The collections of information in 21 CFR part 314 were approved under OMB control numbers 0910–0001 and 0910–0338; the collections of information in 21 CFR part 312 were approved under OMB control number 0910–0014; the collections of information in part 212 were approved under OMB control number 0910–0667; the collections of information in 21 CFR parts 210 and 211 were approved under 0910–0139; and the collections of information in 21 CFR part 207 were approved under OMB control number 0910–0045. The guidance also refers to collections of information associated with submitting Form FDA 3397 (Prescription Drug User Fee Cover Sheet), approved under OMB control number 0910–0297. IV. Electronic Access Persons with access to the Internet may obtain the document at either https://www.fda.gov/Drugs/Guidance ComplianceRegulatoryInformation/ Guidances/default.htm or https:// www.regulations.gov. Products.’’ The document was published with an incorrect email address. This document corrects that error. Due to this error, FDA is extending the Requests for Oral Presentations registration date from November 27, 2012, to December 7, 2012. Lee Lemley, Center for Drug Evaluation and Research, Food and Drug Administration, 10903 New Hampshire Ave. Silver Spring, MD 20903, 301– 796–3441, Fax: 301–847–8753, email: CDER-AntisepticPreOpPublicMeeting@ fda.hhs.gov. SUPPLEMENTARY INFORMATION: FOR FURTHER INFORMATION CONTACT: Correction In the Federal Register of November 21, 2012, in FR Doc. 2012–28357, on page 69863, the following corrections are made: 1. On page 69863, in the second column, under Contact Person, the email address ‘‘AntisepticPreOpPublic Meeting@fda.hhs.gov’’ is corrected to read ‘‘CDER-AntisepticPreOpPublic Meeting@fda.hhs.gov’’. 2. On page 69863, in the third column, under Requests for Oral Presentations, the date ‘‘November 27, 2012’’ is changed to read ‘‘December 7, 2012. Dated: November 28, 2012. Leslie Kux, Assistant Commissioner for Policy. [FR Doc. 2012–29166 Filed 12–3–12; 8:45 am] BILLING CODE 4160–01–P Dated: November 28, 2012. Leslie Kux, Assistant Commissioner for Policy. BILLING CODE 4160–01–P Food and Drug Administration [Docket No. FDA–2012–N–0001] DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration [Docket No. FDA–2012–N–1040] Antiseptic Patient Preoperative Skin Preparation Products; Public Hearing; Request for Comments; Correction Food and Drug Administration, Request for Notification From Industry Organizations Interested in Participating in the Selection Process for Nonvoting Industry Representatives and Request for Nominations for Nonvoting Industry Representatives on the Device Good Manufacturing Practice Advisory Committee HHS. AGENCY: Notice of public hearing; request for comments; correction. mstockstill on DSK4VPTVN1PROD with Food and Drug Administration, HHS. ACTION: The Food and Drug Administration (FDA) is correcting a document that appeared in the Federal Register of November 21, 2012 (77 FR 69863). The document announced a public hearing entitled ‘‘Antiseptic Patient Preoperative Skin Preparation SUMMARY: VerDate Mar<15>2010 17:31 Dec 03, 2012 Jkt 229001 Section 520 of the Federal Food, Drug and Cosmetic Act (21 U.S.C. 360j), as amended, provides that the DGMPAC shall be composed of two representatives of interests of the device manufacturing industry. The Agency is requesting nominations for nonvoting industry representatives on the DGMPAC. SUPPLEMENTARY INFORMATION: I. Function of DGMPAC DEPARTMENT OF HEALTH AND HUMAN SERVICES [FR Doc. 2012–29157 Filed 12–3–12; 8:45 am] AGENCY: Committee (DGMPAC) in the Center for Devices and Radiological Health notify FDA in writing. A nominee may either be self-nominated or nominated by an organization to serve as a nonvoting industry representative. Nominations will be accepted for current vacancies effective with this notice. DATES: Any industry organizations interested in participating in the selection of an appropriate nonvoting members to represent industry interests must send a letter stating that interest to FDA by January 3, 2013, for the vacancies listed in this notice. Concurrently, nomination materials for prospective candidates should be sent to FDA by January 3, 2013. ADDRESSES: All letters of interest and nominations should be submitted in writing to Margaret J. Ames (see FOR FURTHER INFORMATION CONTACT). FOR FURTHER INFORMATION CONTACT: Margaret J. Ames, Center for Devices and Radiological Health, Food and Drug Administration, 10903 New Hampshire Ave., Bldg. 66, Rm. 5234, Silver Spring, MD 20993, 301–796–5960, margaret.ames@fda.hhs.gov. ACTION: Notice. The Food and Drug Administration (FDA) is requesting that any industry organization interested in participating in the selection of nonvoting industry representatives to serve on the Device Good Manufacturing Practice Advisory SUMMARY: PO 00000 Frm 00033 Fmt 4703 Sfmt 4703 Review proposed regulations issuance regarding good manufacturing practices governing the methods used in, and the facilities and controls used for manufacture, packaging, storage, installation, and servicing of devices, and make recommendations regarding the feasibility and reasonableness of those proposed regulations. The committee also reviews and makes recommendations on proposed guidelines developed to assist the medical device industry in meeting the good manufacturing practice requirements, and provides advice with regard to any petition submitted by a manufacturer for an exemption or variance from good manufacturing practice regulations. II. Qualifications Persons nominated for the DGMPAC should possess appropriate qualifications to understand and contribute to the committee’s work as described in the committee’s function. E:\FR\FM\04DEN1.SGM 04DEN1

Agencies

[Federal Register Volume 77, Number 233 (Tuesday, December 4, 2012)]
[Notices]
[Page 71804]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2012-29166]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Food and Drug Administration

[Docket No. FDA-2012-N-1040]


Antiseptic Patient Preoperative Skin Preparation Products; Public 
Hearing; Request for Comments; Correction

AGENCY: Food and Drug Administration, HHS.

ACTION: Notice of public hearing; request for comments; correction.

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SUMMARY: The Food and Drug Administration (FDA) is correcting a 
document that appeared in the Federal Register of November 21, 2012 (77 
FR 69863). The document announced a public hearing entitled 
``Antiseptic Patient Preoperative Skin Preparation Products.'' The 
document was published with an incorrect email address. This document 
corrects that error. Due to this error, FDA is extending the Requests 
for Oral Presentations registration date from November 27, 2012, to 
December 7, 2012.

FOR FURTHER INFORMATION CONTACT: Lee Lemley, Center for Drug Evaluation 
and Research, Food and Drug Administration, 10903 New Hampshire Ave. 
Silver Spring, MD 20903, 301-796-3441, Fax: 301-847-8753, email: CDER-
AntisepticPreOpPublicMeeting@fda.hhs.gov.

SUPPLEMENTARY INFORMATION:

Correction

    In the Federal Register of November 21, 2012, in FR Doc. 2012-
28357, on page 69863, the following corrections are made:
    1. On page 69863, in the second column, under Contact Person, the 
email address ``AntisepticPreOpPublicMeeting@fda.hhs.gov'' is corrected 
to read ``CDER-AntisepticPreOpPublicMeeting@fda.hhs.gov''.
    2. On page 69863, in the third column, under Requests for Oral 
Presentations, the date ``November 27, 2012'' is changed to read 
``December 7, 2012.

    Dated: November 28, 2012.
Leslie Kux,
Assistant Commissioner for Policy.
[FR Doc. 2012-29166 Filed 12-3-12; 8:45 am]
BILLING CODE 4160-01-P

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