96-23669. Cooperative Agreement for Shellfish and Seafood Safety Assistance Project; Intent to Supplement for Fiscal Year 1996  

  • [Federal Register Volume 61, Number 180 (Monday, September 16, 1996)]
    [Notices]
    [Pages 48706-48707]
    From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
    [FR Doc No: 96-23669]
    
    
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    DEPARTMENT OF HEALTH AND HUMAN SERVICES
    
    Cooperative Agreement for Shellfish and Seafood Safety Assistance 
    Project; Intent to Supplement for Fiscal Year 1996
    
    AGENCY: Food and Drug Administration, HHS.
    
    ACTION: Notice of intent.
    
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    SUMMARY: The Food and Drug Administration (FDA), Center for Food Safety 
    and Applied Nutrition, Office of Seafood, is announcing its intention 
    to supplement the current year of the cooperative agreement with the 
    Interstate Shellfish Sanitation Conference (ISSC) in the amount of 
    $165,000. This money will provide for research of Vibrio vulnificus 
    which, although not normally a threat to healthy individuals, can cause 
    serious illness and death in individuals with certain preexisting 
    conditions. The research is intended to provide information to 
    establish science-based controls to protect at-risk consumers from V. 
    vulnificus infection.
    
    ADDRESSES: An application form is available from, and the completed 
    form should be submitted to Robert L. Robins, Division of Contracts and 
    Procurement Management (HFA-520), Food and Drug Administration, Park 
    Bldg., 5600 Fishers Lane, rm. 3-40, Rockville, MD 20857, 301-443-6170. 
    Applications hand-carried or commercially delivered should be addressed 
    to the Park Bldg., 12420 Parklawn Dr., rm. 3-40, Rockville, MD 20857.
    
    FOR FURTHER INFORMATION CONTACT: 
        Regarding the administrative and financial management aspects of 
    this notice: Robert L. Robins (address above).
        Regarding the programmatic aspects of this notice: Paul W. 
    DiStefano, Office of Seafood, Center for Food Safety and Applied 
    Nutrition (HFS-417), Food and Drug Administration, 200 C St. SW., 
    Washington, DC 20204, 202-418-3177.
    
    SUPPLEMENTARY INFORMATION: This project is authorized under section 301 
    of the Public Health Service Act (42 U.S.C. 241). This activity is 
    generally described in the Catalog of Federal Domestic Assistance at 
    93.103. This application is not subject to review as governed by 
    Executive Order 12372, Intergovernmental Review of Federal Program (45 
    CFR 100). Under this supplement, the ISSC will make funds available to 
    State agencies, academic institutions, and private and public 
    organizations for V. vulnificus research through a competitive process.
    
    I. Restricted Eligibility
    
        On October 20, 1995, the Commissioner of Food and Drugs, as 
    authorized by the Public Health Service (PHS) Grants Administration 
    Manual, Part 144.3, determined that a single source cooperative 
    agreement could be awarded to the ISSC without competition. This 
    supplemental application will provide for the implementation and 
    enhancement of activities associated with V. vulnificus described and 
    authorized under the original application, FD-U-000891-01 dated January 
    4, 1996.
    
    II. Availability of Funds
    
        FDA will fund this supplement to the cooperative agreement at a 
    total level of $165,000. The original cooperative agreement has an 
    additional 4 years of support which are contingent upon the 
    availability of fiscal year appropriations, continued support from 
    other government agencies, and successful performance. FDA anticipates 
    that this supplement to the cooperative agreement will commence on or 
    before September 30, 1996.
    
    III. Background
    
        V. vulnificus is a pathogen found in the estuarine environment. V. 
    vulnificus bacteria are not normally a threat to healthy individuals. 
    However, in individuals with preexisting chronic medical conditions 
    such as liver disease, alcoholism, and hemochromatosis, V. vulnificus 
    can cause serious illness and death. Each year, between 12 and 31 cases 
    of V. vulnificus illness associated with consumption of raw molluscan 
    shellfish are reported to public health authorities in the United 
    States.
        The paucity of scientific data associated with V. vulnificus has 
    hindered efforts by public health officials, including FDA, to 
    establish science based controls to protect at-risk consumers from V. 
    vulnificus infection.
    
    IV. Purpose
    
        This supplement to FDA's current cooperative agreement will enable 
    the ISSC to award, through a competitive process, V. vulnificus 
    research projects. Research efforts made possible by this supplement 
    will complement existing efforts under FDA's current cooperative 
    agreement with the ISSC and provide public health officials with better 
    science and an enhanced understanding of V. vulnificus. Innovative 
    research efforts will contribute significantly to the ISSC's and to 
    FDA's ability to identify scientifically defensible controls that will 
    help to reduce the incidence of V. vulnificus illness.
    
    V. Substantive Involvement by FDA
    
        FDA will collaborate with the ISSC in the preparation of the 
    Requests For Application and any other solicitation materials. FDA will 
    review and comment on the methods of solicitation as proposed by the 
    ISSC, provide technical assistance in the form of guidance and 
    participation in the competitive review of all applications, and 
    collaborate with the ISSC in the final selection of subgrantees.
        In the event that the ISSC does not have written policies governing 
    the objective review for awarding subgrants, the ISSC has agreed to 
    adhere to the PHS Grant Policy Statement governing ``Objective Review'' 
    to the extent that it is applicable. All decisions by the objective 
    review panel are final and are not appealable.
    
    VI. Review Procedure and Evaluation Criteria
    
    A. Review Procedure
    
        The application submitted by the ISSC will undergo a noncompetitive 
    dual peer review. The application will be reviewed for scientific and 
    technical merit by a panel of experts based upon applicable evaluation 
    criteria. If the application is recommended for approval, it will then 
    be presented to the National Advisory Environmental Health Sciences 
    Council.
    
    B. Evaluation Criteria
    
        The application will be reviewed and evaluated according to the 
    following criteria:
        1. The application must clearly present an understanding of the 
    purpose and objectives of the supplement to the cooperative agreement 
    in conducting V. vulnificus research and set out the steps, with a 
    proposed schedule for planning, implementing, and accomplishing the 
    activities, to be carried out under this project.
        2. The application must describe the ISSC's ability to perform its 
    responsibilities under this project by providing qualified staff. The
    
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    application must also demonstrate that the ISSC has the financial and 
    other resources required for this project.
        3. The application must specify the approach that the ISSC will use 
    to solicit proposals for V. vulnificus research.
        4. The ISSC application must explain how the ISSC will monitor the 
    progress of selected research projects, and how it will keep FDA 
    informed of any significant advances in the understanding of or control 
    of V. vulnificus.
        In addition, FDA will determine whether the estimated cost of the 
    project is reasonable. The application must include a detailed budget 
    that shows: (1) Anticipated costs for personnel, travel, communications 
    and postage, equipment, and supplies; and (2) the sources of funds to 
    meet those needs.
    
    VII. Reporting Requirement
    
        All terms and conditions of the current award shall remain in full 
    force and effect for the supplemental award.
        As a result of this supplemental award, annual project progress 
    reports must also include the following:
        1. Listing of research projects funded.
        2. Specific purpose of each project.
        3. Cost of each project.
        4. Anticipated completion and milestone dates for each project.
        5. Year-to-date results/scientific findings/public health findings 
    of each project.
        6. Potential V. vulnificus control measures/strategies suggested by 
    research efforts.
    
    VIII. Mechanism of Support
    
        Support for this project will be in the form of a supplement to 
    FDA's cooperative agreement with the ISSC. This agreement will be 
    subject to all policies and requirements that govern the research grant 
    programs of the PHS, including provisions of 42 CFR part 52 and 45 CFR 
    part 74.
    
        Dated: September 10, 1996.
    William K. Hubbard,
    Associate Commissioner for Policy Coordination.
    [FR Doc. 96-23669 Filed 9-13-96; 8:45 am]
    BILLING CODE 4160-01-F
    
    
    

Document Information

Published:
09/16/1996
Department:
Health and Human Services Department
Entry Type:
Notice
Action:
Notice of intent.
Document Number:
96-23669
Pages:
48706-48707 (2 pages)
PDF File:
96-23669.pdf