99-10847. Delegation of Authority and Organization; Center for Veterinary Medicine; Technical Amendment  

  • [Federal Register Volume 64, Number 83 (Friday, April 30, 1999)]
    [Rules and Regulations]
    [Pages 23184-23185]
    From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
    [FR Doc No: 99-10847]
    
    
    =======================================================================
    -----------------------------------------------------------------------
    
    DEPARTMENT OF HEALTH AND HUMAN SERVICES
    
    Food and Drug Administration
    
    21 CFR Part 5
    
    
    Delegation of Authority and Organization; Center for Veterinary 
    Medicine; Technical Amendment
    
    AGENCY: Food and Drug Administration, HHS.
    
    ACTION: Final rule; technical amendment.
    
    -----------------------------------------------------------------------
    
    SUMMARY: The Food and Drug Administration (FDA) is amending the 
    regulation to reflect a redelegation of authority with respect to 
    approval of supplemental new animal drug applications to the Director, 
    Division of Manufacturing Technology, Office of New Animal Drug 
    Evaluation, Center for Veterinary Medicine (CVM). This action is 
    necessary to ensure the continued accuracy of the regulation.
    
    EFFECTIVE DATE: December 22, 1998.
    
    FOR FURTHER INFORMATION CONTACT:
         Carol Haley, Center for Veterinary Medicine (HFV-6), Food and Drug 
    Administration, 7500 Standish Pl., Rockville, MD 20855, 301-594-1682;
         Donna G. Page, Division of Management Systems and Policy (HFA-
    340), Food and Drug Administration, 5600 Fishers Lane, Rockville, MD 
    20857, 301-827-4816.
    
    SUPPLEMENTARY INFORMATION: In the Federal Register of December 22, 1998 
    (63 FR 70650), FDA amended the regulation for redelegations of 
    authority to incorporate provisions for feed mill licensing and to 
    update positions and component titles associated with the authorities 
    under Sec. 5.83 (21 CFR 5.83). The regulation in Sec. 5.83(c)(1) 
    reflected a redelegation with respect to approval of certain 
    supplemental new animal drug applications to the position title 
    ``Director, Division of Human Food Safety, Office of New Animal Drug 
    Evaluation, CVM.'' The correct position title to which these functions 
    should have been redelegated is the ``Director, Division of 
    Manufacturing Technologies, Office of New Animal Drug Evaluation, 
    CVM,'' because that office is responsible for supplemental applications 
    for manufacturing. Therefore, the redelegation to the ``Director, 
    Division of Human Safety Office of New Animal Drug Evaluation, CVM'' 
    has been amended and a new redelegation made to the ``Director, 
    Division of Manufacturing Technologies, Office of New Animal Drug 
    Evaluation, CVM.'' The regulation in Sec. 5.83(c)(1) has been revised 
    to reflect this redelegation. Further redelegation of authorities is 
    not authorized at this time. Authority delegated to a position may be 
    exercised by a person officially designated to serve in such position 
    in an acting capacity or on a temporary basis.
    
    List of Subjects in 21 CFR Part 5
    
         Authority delegations (Government agencies), Imports, Organization 
    and functions (Government agencies).
         Therefore, under the Federal Food, Drug, and Cosmetic Act and 
    under authority delegated to the Commissioner of Food and Drugs, 21 CFR 
    part 5 is amended to read as follows:
    
    PART 5--DELEGATIONS OF AUTHORITY AND ORGANIZATION
    
         1. The authority citation for 21 CFR part 5 continues to read as 
    follows:
    
        Authority: 5 U.S.C. 504, 552, App. 2; 7 U.S.C. 138a, 2271; 15 
    U.S.C. 638, 1261-1282, 3701-3711a; 15 U.S.C. 1451-1461; 21 U.S.C. 
    41-50, 61-63, 141-149, 321-394, 467f, 679(b), 801-886, 1031-1309; 35 
    U.S.C. 156; 42 U.S.C. 241, 242, 242a, 242l, 242n, 243, 262, 263, 
    264, 265, 300u-300u-5, 300aa-1; 1395y, 3246b, 4332, 4831(a), 10007-
    10008; E.O. 11921, 41 FR 24294, 3 CFR 1977 Comp., p. 124-131; E.O. 
    12591, 52 FR 13414, 3 CFR, 1988 Comp., p. 220-223.
    
         2. Section 5.83 is amended by revising paragraph (c)(1) to read as 
    follows:
    
    
    Sec. 5.83   Approval of new animal drug applications, medicated feed 
    mill license applications, and their supplements.
    
    * * * * *
         (c) * * *
         (1) The Director, Division of Manufacturing Technologies, Office 
    of New Animal Drug Evaluation, CVM.
    * * * * *
    
    
    [[Page 23185]]
    
    
        Dated: April 23, 1999.
    William K. Hubbard,
    Acting Deputy Commissioner for Policy.
    [FR Doc. 99-10847 Filed 4-29-99; 8:45 am]
    BILLING CODE 4160-01-F
    
    
    

Document Information

Effective Date:
12/22/1998
Published:
04/30/1999
Department:
Food and Drug Administration
Entry Type:
Rule
Action:
Final rule; technical amendment.
Document Number:
99-10847
Dates:
December 22, 1998.
Pages:
23184-23185 (2 pages)
PDF File:
99-10847.pdf
CFR: (1)
21 CFR 5.83