FDA Support for Conferences and Scientific Meetings (R13 Clinical Trial Not Allowed)
ID: 344880Type: Posted
Overview

Buyer

Food and Drug Administration (HHS-FDA)

Eligible Applicants

Others

Funding Category

Health

Funding Instrument

Grant

Opportunity Category

Discretionary

Cost Sharing or Matching Requirement

Yes

Original Source

https://grants.gov/search-results-detail/344880

Additional Information

https://grants.nih.gov/grants/guide/pa-files/PAR-23-072.html
Timeline
    Description

    The Food and Drug Administration (FDA) is offering a grant opportunity titled "FDA Support for Conferences and Scientific Meetings (R13 Clinical Trial Not Allowed)" aimed at facilitating high-quality conferences and scientific meetings that align with the FDA's public health mission. The program seeks to provide federal financial assistance for events such as symposia, workshops, and seminars, which are essential for exchanging information on topics impacting public health. With an estimated total program funding of $1,000,000 and an expected 20 awards, applicants must submit a Letter of Intent at least eight weeks prior to the application deadlines, which occur in April and October each year until 2025. For further inquiries, interested parties can contact Janelle Fundersburg at janelle.fundersburg@fda.hhs.gov or by phone at 301-798-2533.

    Files
    Title
    Posted
    PAR-23-072_ FDA Support for Conferences...pdf
    PAR-23-072_.pdf
    The file pertains to the process of issuing Requests for Proposals (RFPs) and federal grants at local and state levels, which are essential mechanisms for government entities to procure services or funding for various projects. It outlines the regulations, criteria, and procedures involved in creating and submitting RFPs to ensure transparency and fairness in the selection process. Furthermore, the document emphasizes the importance of compliance with both federal and state laws while managing funds and executing awarded contracts. It discusses key aspects such as eligibility, evaluation criteria, proposal submission guidelines, and reporting obligations for grant recipients. The primary goal of these RFPs and grants is to promote accountability, achieve strategic objectives, and drive community development through effective collaboration with private and non-profit sectors. Overall, the document serves as a foundational guide for stakeholders engaged in government funding processes, ensuring that projects align with public interest and regulatory requirements.
    PAR-23-072.html
    The U.S. Food and Drug Administration (FDA) has announced a Funding Opportunity Announcement (FOA) to support high-quality conferences and scientific meetings through the R13 Clinical Trial Not Allowed grant mechanism. This program aims to align with the FDA's public health mission by financially assisting events such as symposia and workshops. Applicants must secure advance permission to submit grant applications by sending a Letter of Intent at least eight weeks before the application due dates, scheduled for April and October each year until 2025. Funding levels vary by FDA components, with specific caps on total costs for different centers, including up to $250,000 for the Center for Biologics Evaluation and Research (CBER) and unlimited for the Center for Devices and Radiological Health (CDRH). The FOA emphasizes diversity and inclusion in conference planning and requires a detailed diversity plan to enhance participation from underrepresented groups. Applicants are advised to submit applications early to allow for error corrections before the deadline, as late submissions will not be accepted. The document outlines detailed eligibility requirements, application procedures, and review criteria that emphasize scientific merit, innovation, and appropriateness of the conference objectives.
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