97-21585. Delegations of Authority and Organization; Center for Veterinary Medicine  

  • [Federal Register Volume 62, Number 157 (Thursday, August 14, 1997)]
    [Rules and Regulations]
    [Page 43471]
    From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
    [FR Doc No: 97-21585]
    
    
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    DEPARTMENT OF HEALTH AND HUMAN SERVICES
    
    Food and Drug Administration
    
    21 CFR Part 5
    
    
    Delegations of Authority and Organization; Center for Veterinary 
    Medicine
    
    AGENCY: Food and Drug Administration, HHS.
    
    ACTION: Final rule.
    
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    SUMMARY: The Food and Drug Administration (FDA) is amending the 
    regulations for delegations of authority to reflect a new delegation 
    that authorizes the Director and Deputy Director, Center for Veterinary 
    Medicine (CVM), to sign certain Federal Register documents related to 
    the implementation of the Animal Medicinal Drug Use Clarification Act 
    of 1994 (the AMDUCA), as amended hereinafter. This authority will 
    enable the agency to issue Federal Register documents related to 
    implementation of the AMDUCA more efficiently.
    
    EFFECTIVE DATE: August 14, 1997.
    FOR FURTHER INFORMATION CONTACT: 
        Richard L. Arkin, Office of Policy and Regulations (HFV-6), Center 
    for Veterinary Medicine, Food and Drug Administration, 7500 Standish 
    Pl., Rockville, MD 20855-2773, 301-594-1737, or
        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: The regulations are being amended in subpart 
    B of part 5 (21 CFR part 5) by adding a new Sec. 5.40 Issuance of 
    Federal Register documents pertaining to the determination of safe 
    levels, notice of need for development of an analytical method, notice 
    of availability of a developed analytical method, and prohibition of 
    certain extralabel drug use to reflect a new delegation that authorizes 
    the Director and Deputy Director, CVM, to sign certain Federal Register 
    documents related to the implementation of the AMDUCA (Pub. L. 103-
    396), as amended hereinafter. This delegation will permit the efficient 
    implementation of the AMDUCA which was signed into law on October 22, 
    1994.
        This authority may be further redelegated by the Director and 
    Deputy Director, CVM. Authority delegated to a position by title may be 
    exercised by a person officially designated to serve in such a 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 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; secs. 2-12 of the Fair Packaging 
    and Labeling Act (15 U.S.C. 1451-1461); 21 U.S.C. 41-50, 61-63, 141-
    149, 467f, 679(b), 801-886, 1031-1309; secs. 201-903 of the Federal 
    Food, Drug, and Cosmetic Act (21 U.S.C. 321-394); 35 U.S.C. 156; 
    secs. 301, 302, 303, 307, 310, 311, 351, 352, 361, 362, 1701-1706, 
    2101 of the Public Health Service Act (42 U.S.C. 241, 242, 242a, 
    242l, 242n, 243, 262, 263, 264, 265, 300u-300u-5, 300aa-1); 42 
    U.S.C. 1395y, 3246b, 4332, 4831(a), 10007-10008; E.O. 11490, 11921, 
    and 12591.
    
        2. New Sec. 5.40 is added to subpart B to read as follows:
    
    
    Sec. 5.40  Issuance of Federal Register documents pertaining to the 
    determination of safe levels, notice of need for development of an 
    analytical method, notice of availability of a developed analytical 
    method, and prohibition of certain extralabel drug use.
    
        The Director and Deputy Director, Center for Veterinary Medicine 
    (CVM) are authorized to issue Federal Register documents pertaining to 
    the determination of safe levels, notice of need for development of an 
    analytical method, notice of availability of a developed analytical 
    method, and prohibition of certain extralabel drug use related to 
    implementation of the Animal Medicinal Drug Use Clarification Act of 
    1994 (the AMDUCA) (Pub. L. 103-396). This authority may be further 
    redelegated by the Director and Deputy Director, CVM.
    
        Dated: August 8, 1997.
    William K. Hubbard,
    Associate Commissioner for Policy Coordination.
    [FR Doc. 97-21585 Filed 8-13-97; 8:45 am]
    BILLING CODE 4160-01-F
    
    
    

Document Information

Effective Date:
8/14/1997
Published:
08/14/1997
Department:
Food and Drug Administration
Entry Type:
Rule
Action:
Final rule.
Document Number:
97-21585
Dates:
August 14, 1997.
Pages:
43471-43471 (1 pages)
PDF File:
97-21585.pdf
CFR: (1)
21 CFR 5.40