FDA proposes higher fees for drug approvals to cover postmarketing surveillanceBMJ 2007; 334 doi: https://doi.org/10.1136/bmj.39104.352616.DB (Published 25 January 2007) Cite this as: BMJ 2007;334:177
- Janice Hopkins Tanne
- 1New York
The US Food and Drug Administration has agreed with pharmaceutical manufacturers on an almost 30% increase in the “user fees” that drug makers pay to the FDA to expedite approval of new drugs. The FDA has also consulted patient advocates, consumer groups, health professionals, and academic researchers about the new rules.
User fees are annual fees paid by pharmaceutical manufacturers. The FDA wants them to increase by $87.4m to $392.8m (£199.0m; €303.7m). The FDA now gets more than half of its funding from user fees.
The agency will hold a public meeting in Washington, DC, on 16 February to hear comments and will then ask Congress to approve the new rules.
The FDA says the largest portion of the new fees—$29.3m—will …
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