After many months of negotiations with the Food and Drug Administration, the USA’s pharmaceutical industry is close to agreeing reauthorization of the Prescription Drug User Fee Act (PDUFA), last updated in 2007, for a further five years, with a draft agreement published by the FDA last week.
Under the draft accord, the FDA has agreed to PDUFA V recommendations that will enhance the drug development and review process through increased transparency and scientific dialogue, advance regulatory science and strengthen post-market surveillance. For its part, the industry – which provides some 60% of the FDA’s drug review costs - has accepted a 6% rise in user fees to finance the agency’s operations.
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