Memorandum of Understanding Between the Food and Drug Administration and the Association of American Feed Control Officials, 65042-65046 [07-5748]

Download as PDF 65042 Federal Register / Vol. 72, No. 222 / Monday, November 19, 2007 / Notices TABLE 1.—ESTIMATED ANNUAL REPORTING BURDEN1 21 CFR Part 710 No. of Respondents Form FDA 2511 1There 135 Dated: November 13, 2007. Jeffrey Shuren, Assistant Commissioner for Policy. [FR Doc. E7–22588 Filed 11–16–07; 8:45 am] BILLING CODE 4160–01–S DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration [Docket No. 2006F–0058] ARCH Chemicals, Inc.; Withdrawal of Food Additive Petition FAP 6B4764 AGENCY: Food and Drug Administration, HHS. 1 Hours per Response 135 Total Hours 0.2 Notice. antimicrobial agent in the manufacture of food-contact paper and paperboard. 27 DEPARTMENT OF HEALTH AND HUMAN SERVICES FOR FURTHER INFORMATION CONTACT: Food and Drug Administration Elizabeth S. Furukawa, Center for Food Safety and Applied Nutrition (HFS– 275), Food and Drug Administration, 5100 Paint Branch Pkwy., College Park, MD 20740–3835, 301–436–1216, e-mail: Elizabeth.Furukawa@fda.hhs.gov. In a notice published in the Federal Register of February 15, 2006 (71 FR 7975), FDA announced that a food additive petition (FAP 6B4764) had been filed by ARCH Chemicals, Inc., 1955 Lake Park Dr., suite 100, Smyrna, GA 30080. The petition proposed to amend the food additive regulations in 21 CFR 176.170 Components of paper and paperboard in contact with aqueous and fatty foods and 21 CFR 176.180 Components of paper and paperboard in contact with dry food to provide for the safe use of poly (iminoimidocarbonyliminoimido carbonyliminohexamethylene) hydrochloride (CAS Reg. No. 32289–58– 0) as an antimicrobial agent in the manufacture of food-contact paper and paperboard. ARCH Chemicals, Inc., has now withdrawn the petition without prejudice to a future filing (21 CFR 171.7). SUPPLEMENTARY INFORMATION: Dated: November 9, 2007. Laura M. Tarantino, Director, Office of Food Additive Safety, Center for Food Safety and Applied Nutrition. [FR Doc. E7–22536 Filed 11–16–07; 8:45 am] BILLING CODE 4160–01–S The Food and Drug Administration (FDA) is announcing the withdrawal, without prejudice to a future filing, of a food additive petition (FAP 6B4764) proposing that the food additive regulations be amended to provide for the safe use of poly (iminoimidocarbonyliminoimidocarbon yliminohexamethylene) hydrochloride (CAS Reg No. 32289–58–0) as an SUMMARY: rwilkins on PROD1PC63 with NOTICES Total Annual Responses are no capital costs or operating and maintenance costs associated with this collection of information. FDA bases its estimate on its review of the registrations received over the past 3 fiscal years. The total annual responses (averaged over fiscal years 2004 through 2006) is 9 times the previous total reported in 2004 (for fiscal years 2000 through 2003) due to increased participation by cosmetic companies, because of a renewed industry commitment to the program, and implementation of the online registration system on December 1, 2005. Due to the ease of online registration, FDA estimates that the hours per response have declined from 0.4 hours to 0.2 hours. Thus, the total estimated hour burden for this information collection is 27 hours, which is 4.5 times the previous level reported in 2004. ACTION: Annual Frequency per Response VerDate Aug<31>2005 20:17 Nov 16, 2007 Jkt 214001 PO 00000 [FDA 225–07–7001] Memorandum of Understanding Between the Food and Drug Administration and the Association of American Feed Control Officials AGENCY: Food and Drug Administration, HHS. ACTION: Notice. SUMMARY: The Food and Drug Administration (FDA) is providing notice of a memorandum of understanding (MOU) between FDA and the Association of American Feed Control Officials (AAFCO). The purpose of this MOU is to facilitate FDA’s collaboration with AAFCO in the AAFCO New and Modified Ingredient Definition Process by clarifying the responsibilities of FDA and AAFCO in defining feed ingredients, in providing mechanisms for resolving disputes that may arise, and in providing mechanisms for modifying the ingredient definition process when required. DATES: The agreement became effective August 30, 2007. FOR FURTHER INFORMATION CONTACT: Sharon Benz, Division of Animal Feeds (HFV–220), Center for Veterinary Medicine, Food and Drug Administration, 7519 Standish Pl., Rockville, MD 20855, 240–453–6864. SUPPLEMENTARY INFORMATION: In accordance with 21 CFR 20.108(c), which states that all written agreements and MOUs between FDA and others shall be published in the Federal Register, the agency is publishing notice of this MOU. Dated: November 12, 2007. Randall W. Lutter, Deputy Commissioner for Policy. BILLING CODE 4160–01–S Frm 00057 Fmt 4703 Sfmt 4703 E:\FR\FM\19NON1.SGM 19NON1 VerDate Aug<31>2005 20:17 Nov 16, 2007 Jkt 214001 PO 00000 Frm 00058 Fmt 4703 Sfmt 4725 E:\FR\FM\19NON1.SGM 19NON1 65043 EN19NO07.016</GPH> rwilkins on PROD1PC63 with NOTICES Federal Register / Vol. 72, No. 222 / Monday, November 19, 2007 / Notices VerDate Aug<31>2005 Federal Register / Vol. 72, No. 222 / Monday, November 19, 2007 / Notices 20:17 Nov 16, 2007 Jkt 214001 PO 00000 Frm 00059 Fmt 4703 Sfmt 4725 E:\FR\FM\19NON1.SGM 19NON1 EN19NO07.017</GPH> rwilkins on PROD1PC63 with NOTICES 65044 VerDate Aug<31>2005 20:17 Nov 16, 2007 Jkt 214001 PO 00000 Frm 00060 Fmt 4703 Sfmt 4725 E:\FR\FM\19NON1.SGM 19NON1 65045 EN19NO07.018</GPH> rwilkins on PROD1PC63 with NOTICES Federal Register / Vol. 72, No. 222 / Monday, November 19, 2007 / Notices 65046 Federal Register / Vol. 72, No. 222 / Monday, November 19, 2007 / Notices BILLING CODE 4160–01–C DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration [Docket No. 2007D–0449] Draft Guidance for Food and Drug Administration Advisory Committee Members and Food and Drug Administration Staff: Voting Procedures for Advisory Committee Meetings; Availability rwilkins on PROD1PC63 with NOTICES AGENCY: Food and Drug Administration, Notice. 20:17 Nov 16, 2007 Submit written requests for single copies of the guidance to the Office of Policy (HF–11), Office of the Commissioner, Food and Drug ADDRESSES: The Food and Drug Administration (FDA) is announcing the availability of a draft guidance SUMMARY: VerDate Aug<31>2005 Although you can comment on any guidance at any time (see 21 CFR 10.115(g)(5)), to ensure that the agency considers your comment on this draft guidance before it begins work on the final version of the guidance, submit written or electronic comment on the draft guidance by January 18, 2007. DATES: HHS. ACTION: document for FDA advisory committee members and FDA staff entitled, ‘‘Voting Procedures for Advisory Committee Meetings.’’ This draft document is intended to provide guidance on advisory committee voting procedures that can be used for the voting process when votes are taken during advisory committee meetings. It does not to define when votes should be taken. Jkt 214001 PO 00000 Frm 00061 Fmt 4703 Sfmt 4703 Administration, 5600 Fishers Lane, Rockville, MD 20857. Send one selfaddressed adhesive label to assist that office in processing your requests. Submit phone requests to 800–835–4709 or 301–827–1800. Submit written comments on the guidance to the Division of Dockets Management (HFA– 305), Food and Drug Administration, 5630 Fishers Lane, rm. 1061, Rockville, MD 20852. Submit electronic comments to https://www.fda.gov/dockets/ ecomments or https:// www.regulations.gov. See the SUPPLEMENTARY INFORMATION section for electronic access to the guidance document. Jill Hartzler Warner, Office of Policy, Planning, and Preparedness (HF–11), Food and Drug Administration, 5600 Fishers Lane, Rockville, MD 20857, 301–827–3370. FOR FURTHER INFORMATION CONTACT: E:\FR\FM\19NON1.SGM 19NON1 EN19NO07.019</GPH> [FR Doc. 07–5748 Filed 11–16–07; 8:45 am]

Agencies

[Federal Register Volume 72, Number 222 (Monday, November 19, 2007)]
[Notices]
[Pages 65042-65046]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 07-5748]


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

DEPARTMENT OF HEALTH AND HUMAN SERVICES

Food and Drug Administration

[FDA 225-07-7001]


Memorandum of Understanding Between the Food and Drug 
Administration and the Association of American Feed Control Officials

AGENCY: Food and Drug Administration, HHS.

ACTION: Notice.

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

SUMMARY: The Food and Drug Administration (FDA) is providing notice of 
a memorandum of understanding (MOU) between FDA and the Association of 
American Feed Control Officials (AAFCO). The purpose of this MOU is to 
facilitate FDA's collaboration with AAFCO in the AAFCO New and Modified 
Ingredient Definition Process by clarifying the responsibilities of FDA 
and AAFCO in defining feed ingredients, in providing mechanisms for 
resolving disputes that may arise, and in providing mechanisms for 
modifying the ingredient definition process when required.

DATES:  The agreement became effective August 30, 2007.

FOR FURTHER INFORMATION CONTACT:  Sharon Benz, Division of Animal Feeds 
(HFV-220), Center for Veterinary Medicine, Food and Drug 
Administration, 7519 Standish Pl., Rockville, MD 20855, 240-453-6864.

SUPPLEMENTARY INFORMATION: In accordance with 21 CFR 20.108(c), which 
states that all written agreements and MOUs between FDA and others 
shall be published in the Federal Register, the agency is publishing 
notice of this MOU.

    Dated: November 12, 2007.
Randall W. Lutter,
Deputy Commissioner for Policy.
BILLING CODE 4160-01-S

[[Page 65043]]

[GRAPHIC] [TIFF OMITTED] TN19NO07.016


[[Page 65044]]


[GRAPHIC] [TIFF OMITTED] TN19NO07.017


[[Page 65045]]


[GRAPHIC] [TIFF OMITTED] TN19NO07.018


[[Page 65046]]


[GRAPHIC] [TIFF OMITTED] TN19NO07.019

[FR Doc. 07-5748 Filed 11-16-07; 8:45 am]
BILLING CODE 4160-01-C

This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply.