African Medical Devices Regulatory Harmonization Program
Food and Drug Administration · Department of Health and Human Services · FOR-FD-23-012
In plain English
Food and Drug Administration (Department of Health and Human Services) has announced this as a forecast: an opportunity it expects to post. It is not open for applications yet.
The listing does not state award amounts or the number of awards.
Eligibility is described in the listing text (the "Others" category).
The listing says cost sharing or matching is not required.
Built only from the fields in the Grants.gov listing. Always confirm on the official listing.
Key facts
| Status | Forecasted: not open yet |
|---|---|
| Estimated posting date | Not stated |
| Estimated application due date | Not stated |
| Fiscal year | 2023 |
| Forecast posted | Jul 6, 2022 |
| Opportunity number | FOR-FD-23-012 |
| Agency | Food and Drug Administration (Department of Health and Human Services) |
| Funding instrument | Cooperative agreement |
| Category | Science and Technology and other Research and Development |
| Opportunity category | Discretionary |
| Award ceiling (max per award) | Not stated |
| Award floor (min per award) | Not stated |
| Estimated total program funding | Not stated |
| Expected number of awards | Not stated |
| Cost sharing or matching required | No |
| Assistance listing (CFDA/ALN) | 93.103 – Food and Drug Administration Research |
| Last updated on Grants.gov | Jul 6, 2022 |
Who can apply
- Others (see the eligibility details in the listing)
Additional eligibility information (excerpt from the listing):
Sole Source
Description
Excerpt from the official forecast on Grants.gov (shortened; read the full text on 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.
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