Literature DB >> 15328872

Managing delegation in the FDA: reducing delay in new-drug review.

Mary K Olson1.   

Abstract

This article examines the effects of the user fee reform on the speed of drug review in the U.S. Food and Drug Administration. The results show that even after controlling for increased agency resources, the reform reduced review times among new-drug approvals by 34 percent (95 percent confidence interval, 11 to 51 percent, p = .01). The results suggest that increased agency resources alone cannot explain the reductions in drug-review times. Evidence suggests that other reform-specific factors facilitated the change. Such factors may include the agency's desire to obtain program renewal and secure future fee revenues as well as heightened industry monitoring. Additional results show that there were significant increases in the speed of review for novel drugs in the reform era and for drugs in certain classes that have historically experienced longer delays. The results suggest that the user fee reform has helped politicians manage delegation and reduce delay in new-drug review.

Mesh:

Year:  2004        PMID: 15328872     DOI: 10.1215/03616878-29-3-397

Source DB:  PubMed          Journal:  J Health Polit Policy Law        ISSN: 0361-6878            Impact factor:   2.265


  2 in total

1.  Association Between Food and Drug Administration Advisory Committee Recommendations and Agency Actions, 2008-2015.

Authors:  Audrey D Zhang; Jason L Schwartz; Joseph S Ross
Journal:  Milbank Q       Date:  2019-07-14       Impact factor: 4.911

2.  Survey of Japanese Orphan Drug Program: Factors Related to Successful Marketing Approval.

Authors:  Kenji Harada; Kazuki Toriyabe; Shunsuke Ono
Journal:  J Clin Pharmacol       Date:  2019-07-31       Impact factor: 3.126

  2 in total

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