Forecasted · Cooperative Agreement
African Medical Devices Regulatory Harmonization Program
Food and Drug Administration, Department of Health and Human Services
Key facts
Copied from the official Grants.gov record. Last verified October 29, 2026.
- Program name
- African Medical Devices Regulatory Harmonization Program
- Issuing agency
- Food and Drug Administration (Department of Health and Human Services)
- Opportunity number
- FOR-FD-23-012
- Funding type
- Cooperative Agreement
- Funding purpose
- Science and Technology and other Research and Development
- Status
- Forecasted
- Application deadline
- Forecasted · no application dates yet
- Published award range
- Not published by the agency
- Cost sharing or match required
- No
- Eligible applicants (official categories)
- Others (see Additional Information on Eligibility)
- Relevant to
- Neither businesses nor nonprofits are listed
- Geographic restrictions
- None stated in structured data (federal opportunities are often nationwide). Check the eligibility details and full announcement for any limits.
- Assistance Listing (CFDA)
- 93.103
- Official source
- View on Grants.gov ↗
- Application URL
- www.grants.gov/search-results-detail/341844 ↗Apply through Grants.gov (Workspace) using the application package on the official listing, unless the full announcement names a different submission system.
- Source identifier
- Grants.gov opportunity ID 341844 · Funding opportunity number FOR-FD-23-012
- Posted
- July 6, 2022 · Source last updated July 6, 2022
- Last verified
- October 29, 2026 (against Grants.gov)
- Data completeness
- 83% of key fields published by the sourceNot published: published funding range, application dates.
- Record confidence
- mediumforecast — dates and amounts are agency estimates.
Eligibility details (from the agency)
Sole Source
Description (from the official listing)
The purpose of this program is to enable harmonized approaches, standards and guidelines in order to strengthen innovation, development, regulation and availability of medical devices that meet quality and safety requirements in the African continent. These efforts are critical to ensure consistent and aligned practices for the regulatory oversight of medical devices and to prevent the use or export of poor quality products that can lead to health consequences and increased expenditures.
Agency contact
Shashi Malhotra Grants Management Specialist
shashi.malhotra@fda.hhs.gov