Additional steps must be taken by the US Food and Drug Administration to increase the rate of generics approved after their first review cycle, according to a report to congressional committees made by the US Government Accountability Office. Between 2015 and 2017, the GAO report observes, just 12% of generic applications were approved on the first cycle, with dossiers on average going through three review cycles before being signed off by the FDA, a process that can take several years.
In its report, the GAO acknowledges that the agency has made efforts to get more generics approved on the first...




