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Food & Drug Administration Grants
Vet-LIRN Cooperative Agreement Program to Expand and Validate Testing Methods for Food Contaminants in Animal Diagnostic Specimens (U18)
From - Food & Drug AdministrationDescription - FDA developed the Veterinary Laboratory Investigation and Response Network (Vet- LIRN, formerly Vet-LRN) to increase the safety of human and animal health by investigating potential adverse events...more
Posted On - 2013-06-14
Advancing Medical Device Postmarket Surveillance Infrastructure and Epidemiologic Methodologies through Multi-stakeholder Partnership (U01)
From - Food & Drug AdministrationDescription - 1) To support implementation of the National Medical Device Postmarket Surveillance System through sustainable multi-stakeholder partnership 2) To develop new epidemiologic methodologies or to...more
Posted On - 2013-05-22
National Consumer Food Safety Education Conference (U13)
From - Food & Drug AdministrationDescription - The purpose of the National Consumer Food Safety Education Conference is to advance the knowledge, practice and effectiveness of health and food safety educators in support of two Healthy People 2020...more
Posted On - 2013-05-17
In vitro release tests for transdermal drug delivery systems (U01)
From - Food & Drug AdministrationDescription - Background Many transdermal delivery systems (TDDS) are labeled to warn against applying heat to the TDDS as it may increase the rate of drug release. When the reference product contains these...more
Posted On - 2013-05-07
Development of in vivo predictive dissolution method for orally inhaled drug products
From - Food & Drug AdministrationDescription - Clinical performance of orally inhaled drug products (OIDPs) depends not only on regional drug deposition in the lung but also on in vivo drug dissolution rate, thereby affecting local availability...more
Posted On - 2013-05-07
In vitro release tests for topical dermatological products (U01)
From - Food & Drug AdministrationDescription - Background: Developing appropriate methods to determine bioequivalence of topical dermatological products has been a longstanding challenge to FDA. FDA has begun to identify situations when...more
Posted On - 2013-05-07
Food Protection Task Force Conference (R13)
From - Food & Drug AdministrationDescription - This Funding Opportunity Announcement (FOA), issued by the Food and Drug Administration under the support for Conferences and Scientific meetings Grant mechanism (R13), is to solicit applications...more
Posted On - 2013-05-01
Enhancing post-market surveillance through developing registries for medical device epidemiology (U01)
From - Food & Drug AdministrationDescription - (1) To address identified gaps in the current postmarket surveillance system by developing new methodologies for registry data collection and linkage, or by adapting known methodologies to medical...more
Posted On - 2013-04-19
In vitro-In vivo Correlations of Parenteral Microsphere Drug Products
From - Food & Drug AdministrationDescription - The purpose of this study is to investigate in vitro-in vivo correlations of parenteral microspheres. The encapsulated agent may be a small molecule or peptide, and the dosage form should be an...more
Posted On - 2013-04-18
