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Animal & Veterinary

FDA Announces Minor Use/Minor Species (MUMS) Grant Program Request for Applications due August 15, 2014

June 20, 2014

The Food and Drug Administration today announced the opening date for applications for grants to support the development of new animal drugs intended for minor species or minor uses in major species. (Major species are horses, dogs, cats, cattle, pigs, turkeys and chickens.) Applications must be submitted electronically by August 15, 2014, through

The grant program was established by the Minor Use and Minor Species Animal Health Act of 2004, and funding was authorized to start after finalization of regulations to implement the Designation provisions of Section 573 of the Federal Food, Drug & Cosmetic Act.

Eligibility requirements to apply for a MUMS grant include: 1) the drug must be “designated” by the FDA Center for Veterinary Medicine’s (CVM) Office of Minor Use and Minor Species Animal Drug Development (OMUMS) under the MUMS Act; 2) the grant funding must be used to defray the costs of qualified safety and effectiveness testing expenses associated with the development of the drug for the designated intended use; and 3) interested parties must have a study protocol that has been accepted by CVM’s Office of New Animal Drug Evaluation (ONADE) prior to submitting the grant application. Qualified studies include those intended to support target animal safety or effectiveness, environmental safety, or human food safety. For human food safety, a separate study to validate an analytical method prior to conduct of an in-life study is eligible for funding, if a protocol for the stand-alone method validation study has been accepted by ONADE.

Subject to the availability of funds, grants will be available for up to $75,000 per year for up to two years for routine studies; and up to $125,000 per year for up to two years for studies of unusual complexity, duration or size. A third year of funding may be available for long-term toxicology studies. Therefore, grants could range from under $75,000 for a routine study that could be completed in less than a year, to $250,000 for a complex study requiring two years for completion, to $375,000 for a long-term toxicology study. Indirect costs are limited to 15% of direct costs.

The complete Request for Applications is available at Please note revisions to dates and text in Notice NOT-FD-13-014, at


Contact FDA

240-276-9115 FAX
Issued by: FDA, Center for Veterinary Medicine

7519 Standish Place, HFV-1

Rockville, MD 20855

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