Pilot Studies to Develop and Test Novel, Low- Cost Methods for the Conduct of Clinical Trials (R01)
The summary for the Pilot Studies to Develop and Test Novel, Low- Cost Methods for the Conduct of Clinical Trials (R01) Federal Grant is detailed below.
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Federal Grant Title:
PILOT STUDIES TO DEVELOP AND TEST NOVEL, LOW- COST METHODS FOR THE CONDUCT OF CLINICAL TRIALS (R01)
State governments - County governments - City or township governments - Special district governments - Independent school districts - Public and State controlled institutions of higher education - Native American tribal governments (Federally recognized) - Public housing authorities/Indian housing authorities - Native American tribal organizations (other than Federally recognized tribal governments) - Nonprofits having a 501(c)(3) status with the IRS, other than institutions of higher education - Nonprofits that do not have a 501(c)(3) status with the IRS, other than institutions of higher education - Private institutions of higher education - For profit organizations other than small businesses - Small businesses - Others (see text field entitled "Additional Information on Eligibility" for clarification)
Additional Information on Eligibility
Other Eligible Applicants include the following: Alaska Native and Native Hawaiian Serving Institutions; Eligible Agencies of the Federal Government; Faith-based or Community-based Organizations; Hispanic-serving Institutions; Historically Black Colleges and Universities (HBCUs); Indian/Native American Tribal Governments (Other than Federally Recognized); Regional Organizations; Tribally Controlled Colleges and Universities (TCCUs) ; U.S. Territory or Possession; Non-domestic (non-U.S.) Entities (Foreign Organizations) are not eligible to apply. Foreign (non-U.S.) components of U.S. Organizations are not allowed.
The funding announcement solicits R01 applications that develop and test new, low cost methods to conduct clinical trials. Responsive applicants will address four challenges to the conduct of clinical trials: (1) minimize specialized infrastructure, (2) minimize visits designed solely for the trial, (3) explore novel methods of obtaining consent that minimize burden, and (4) employ low-cost methods of monitoring study conduct. The proposed methodology must be tested in a pilot trial. New and innovative designs that have not been tested in previous studies but hold potential for increasing the efficiency and reducing the cost of conduct of clinical trials are especially encouraged.