Abstract
The role of the Food and Drug Administration (FDA) is to ensure the safety of prescription and nonprescription drugs, dietary supplements, and the food supply, representing more than 20% of US consumer spending. The increased need to monitor imported drugs, drug products and foods, drug shortages, and compounding pharmacies bring the adequacy of FDA funding into question. Performing even at status quo cannot be accomplished if responsibilities increase without equitable funding increases: both from the federal government and fees imposed on FDA-regulated industries. Additionally, scientific advancement, new legislation, and new industries are continually increasing the FDA workload, necessitating commensurate budget increases.
| Original language | American English |
|---|---|
| Pages (from-to) | 57-60 |
| Number of pages | 4 |
| Journal | The Journal of Pharmacy Technology : JPT |
| Volume | 30 |
| Issue number | 2 |
| DOIs | |
| State | Published - Apr 1 2014 |
Bibliographical note
© The Author(s) 2013.Keywords
- FDA
- drug compounding
- funding
- quality control
- regulation
- safety
- Drug compounding
- Funding
- Quality control
- Regulation
- Safety
Disciplines
- Medicine and Health Sciences
- Pharmacy and Pharmaceutical Sciences