Food and Drug Administration, HHS.
The Food and Drug Administration (FDA), Center for Food Safety and Applied Nutrition (CFSAN), Office of Food Safety is announcing its intent to award a single source cooperative agreement to support the Interstate Shellfish Sanitation Conference (ISSC). The purpose of this cooperative agreement is to enhance the FDA molluscan shellfish sanitation program and provide the public greater assurance of the quality and safety of these products.
Important dates are as follows:
1. The application due date is July 15, 2011.
2. The anticipated start date is September 1, 2011.
3. The opening date is June 28, 2011.
4. The expiration date is July 16, 2011.
For Further Information and Additional Requirements Contact:
For Programmatic and Technical Concerns and Questions: Paul DiStefano, Center for Food Safety and Applied Nutrition (HFS-325), Food and Drug Administration, 5100 Paint Branch Pkwy., College Park, MD 20740, 240-402-1410.
For Administrative and Financial Concerns and Questions: Gladys Melendez-Bohler, Office of Acquisitions and Grants Services (HFA-500), Food and Drug Administration, 5630 Fishers Lane, rm. 1078, Rockville, MD 20857, 301-827-7175.End Preamble Start Supplemental Information
I. Funding Opportunity Description
The CFSAN Office of Food Safety is announcing its intent to award, a single source cooperative agreement to the ISSC in the amount of $325,000 for fiscal year 2011, direct and indirect costs combined. Subject to the Start Printed Page 37816availability of Federal funds and successful performance, 4 additional years of support will be available. This effort will enhance FDA's molluscan shellfish sanitation program and provide the public greater assurance of the quality and safety of these products.
Molluscan shellfish have been recognized by FDA as a significant source of seafood-borne illnesses and continue to be the subject of congressional, State, industry, and public concern. FDA has given high priority to enhance the Agency's shellfish safety program and to provide the public greater assurance of the quality and safety of these products. FDA administers the National Shellfish Sanitation Program (NSSP). Under that program the NSSP Model Ordinance serves as guidance for State shellfish sanitation programs and the issuance of State regulations and laws concerning shellfish safety. This cooperative agreement will enhance FDA efforts to help ensure that shellfish is free of harmful pathogens.
B. Research Objectives
This proposed cooperative agreement with ISSC will continue to: (1) Address the need to improve information exchange and transfer among States, Federal Agencies, industry, and consumers; (2) strengthen State activities by providing them with procedural and policy guidance, technical training, research, consumer education, and support for States to participate in ISSC biennial meetings and ISSC committee meetings; and (3) promote efforts and projects, including research, that will contribute significantly to the ability of FDA and States to identify and implement scientifically defensible food safety controls to reduce the risk of illness associated with molluscan shellfish consumption, including Vibrio vulnificus and V. parahaemolyticus. Research efforts will provide information and data that can be used to reduce assumptions and tighten modeling outputs of the V. vulnificus and V. parahaemolyticus risk assessments developed by the Food and Agriculture Organization of the World Health Organization and FDA. Substantive accomplishments of the ISSC under previous cooperative agreements include:
1. Coordination of annual shellfish safety meetings of Federal regulators, State regulators, and industry members for the purpose of developing improved science based shellfish safety controls in the NSSP Model Ordinance for implementation by State shellfish control agencies and the shellfish industry;
2. Facilitation of the incorporation and implementation of Hazard Analysis and Critical Control Point (HACCP) into the NSSP Model Ordinance;
3. Facilitation of an ISSC Unresolved Issues Process to resolve shellfish safety program discrepancies between FDA and States, ensuring continued compliance with NSSP shellfish safety controls;
4. Coordination of NSSP Model Ordinance revisions and electronic online availability;
5. Coordination with FDA on the development and oversight of a V. parahaemolyticus control plan;
6. Development of an educational training video concerning the risks and control of illegal shellfish harvesting;
7. Development of an education training video concerning the public health implications associated with overboard waste discharges from harvest vessels;
8. Development of accredited online training courses for medical professionals concerning Vibrio illness and shellfish consumption;
9. Development and maintenance of a World Wide Web site for continuous accessibility to molluscan shellfish safety information, including up-to-date information regarding outbreaks and recalls;
10. Coordination, development and oversight of a V. vulnificus control plan;
11. In conjunction with FDA, conduct of retail and processing plant product sampling studies to examine Vibrios in molluscan shellfish that have undergone a post harvest process to reduce levels of Vibrios; and;
12. In conjunction with FDA, conduct of a retail shellfish study to look at the occurrence of pathogens in molluscan shellfish, including norovirus, Hepatitis A virus, Salmonella, and Vibrios; and
13. In conjunction with FDA, development of a risk-based approach to evaluating State compliance with NSSP Model Ordinance requirements for controlling the safety of molluscan shellfish.
Other substantive accomplishments of the ISSC include facilitating and coordinating development of shellstock time-temperature controls for V. vulnificus and V. parahaemolyticus; funding support for V. vulnificus virulent strain identification research; funding support to research the effects of ice chilling on V. vulnificus; funding support to research the influence of water and air temperature, dissolved oxygen, and nutrients on V. parahaemolyticus concentrations in Pacific oysters; funding support to conduct an economic assessment of mandating post-harvest treatment of oysters; funding support to conduct a consumer acceptance study of oysters that have been post-harvest treated to reduce Vibrio levels to nondetect; development of a V. vulnificus laboratory methodology training video; and development and broadcast of a public service announcement to alert at risk consumers of the dangers associated raw shellfish consumption.
This project will (1) enhance both the effectiveness and uniformity of the national molluscan shellfish safety program by improving the flow of information between Federal and State regulatory agencies, industry, and consumers; (2) strengthen State activities by providing assistance in such areas as procedural and policy guidance, technical training, research, consumer education, and conformity with requirements of the NSSP Model Ordinance; (3) provide for research opportunities related to shellfish safety; and (4) bring to final resolution the development and implementation by States and industry of effective Vibrio risk control plans that are consistent with current science, epidemiology, and HACCP based food safety measures.
Substantive involvement by FDA will include:
(1) FDA will monitor the ISSC's overall conduct under this cooperative agreement.
(2) FDA will have representation on the ISSC Executive Board, Committees, and Task Forces.
(3) FDA will collaborate and work closely with the ISSC on V. vulnificus and V. parahaemolyticus risk reduction efforts. FDA will continue to monitor State activities to ensure illness/risk reduction goals of the ISSC V. vulnificus control plan are met and continue to monitor State activities to ensure that the ISSC V. parahaemolyticus control plan is fully implemented.
(4) FDA will continue to work with ISSC to develop State program evaluation criteria.
(5) FDA will analyze State shellfish program data and information and work through the ISSC to resolve any State shellfish program problems that may impact public health.
(6) FDA will conduct training courses in growing area classification, plant sanitation, and HACCP and plant standardization for participants of the ISSC, including online training modules.
(7) FDA will work with the ISSC to develop new microbiological and marine biotoxin techniques and to develop and implement early warning systems for toxic algal blooms and new Start Printed Page 37817strategies for managing areas affected by toxic algal blooms.
(8) FDA will continue to work with ISSC to establish improved mechanisms for incorporating new lab methods into the NSSP.
(9) FDA will work with the ISSC to develop NSSP Model Ordinance interpretations.
(10) FDA will take any action that may be necessary to ensure compliance with this cooperative agreement including, but not limited to the pursuit of science-based HACCP controls for managing the risk of Vibrios, and developing patrol, growing area classification, and plant inspection criteria.
C. Eligibility Information
Competition is limited to ISSC because it has unique capacity found nowhere else. ISSC is the primary voluntary National organization of State shellfish regulatory officials that provides guidance and counsel to the States and industry on matters of sanitary control of molluscan shellfish. ISSC is the only organization that has the established formal structure, procedures, and expertise to direct all components (public health, environmental, resource management, and enforcement) of an effective National shellfish safety program, and has operated satisfactorily in this capacity since 1993. This effort will enhance FDA's molluscan shellfish safety program and provide the public greater assurance of the quality and safety of shellfish products.
II. Award Information/Funds Available
A. Award Amount
The annual allocation to the ISSC under this cooperative agreement, including support in the amount of $75,000.00 from the National Marine Fisheries Services will be $325,000.00.
Subject to the availability of Federal funds and successful performance, 4 additional years of support will be available. CFSAN intends to fund 1 year of award to begin in September 1, 2011. Subject to annual appropriations and successful performance, 4 additional years of noncompetitive award will be available.
B. Length of Support
September 1, 2011, to August 31, 2016.
III. Paper Application, Registration, and Submission Information
To submit a paper application in response to the funding opportunity announcement (FOA), applicants should first review the full announcement located at http://www.fda.gov/Food/NewsEvents/default.htm. (FDA has verified the Web site addresses throughout this document, but FDA is not responsible for any subsequent changes to the Web sites after this document publishes in the Federal Register.) Persons interested in applying for a grant may obtain an application at http://grants2.nih.gov/grants/funding/phs398/phs398.html. For all paper application submissions, the following steps are required:
- Step 1: Obtain a Dun and Bradstreet Data Universal Numbering System (DUNS) Number
- Step 2: Register With Central Contractor Registration
- Step 3: Register With Electronic Research Administration (eRA) Commons
Steps 1 and 2, in detail, can be found at http://www07.grants.gov/applicants/organization_registration.jsp. Step 3, in detail, can be found at https://commons.era.nih.gov/commons/registration/registrationInstructions.jsp.
After you have followed these steps, submit paper applications to: Gladys Melendez-Bohler, Office of Acquisition and Grants Services (HFA-500), Food and Drug Administration, 5630 Fishers Lane, rm. 1078, Rockville, MD 20857, 301-827-7175, e-mail: firstname.lastname@example.org.Start Signature
Dated: June 22, 2011.
Acting Assistant Commissioner for Policy.
[FR Doc. 2011-16119 Filed 6-27-11; 8:45 am]
BILLING CODE 4160-01-P