We use cookies to provide you with a better experience. By continuing to browse the site you are agreeing to our use of cookies in accordance with our Cookie Policy.
The data integrity issues most likely to lead to a delay in FDA marketing approval for new drugs include poor quality control for data entry, systemic errors at clinical study sites and database changes made after an initial database lock and study unblinding. Read More
Randomized controlled trials have long been the standard for efficacy claims, but a new report calls on the FDA to lay out terms for using real-world data in the drug approval process. Read More
As the life science industry waits for Brexit to be formalized, regulatory compliance experts foresee a standstill in the country’s research and development. Read More
An FDA advisory committee recommended the approval of Merck’s bezlotoxumab to prevent Clostridium difficile infection recurrence in patients 18 and older. Read More
The FDA is providing recommendations on clinical trial designs for sponsors developing antiviral drugs to prevent and treat herpes-related sores that form around the mouth. Read More
Drugmakers developing treatments for uncomplicated vulvovaginal candidiasis should conduct two adequate and well-controlled clinical trials with a superiority design to demonstrate efficacy, the FDA says. Read More
The FDA is pushing for more uniform quality assessments in the clinical development of chewable tablets after finding significant variation among manufacturers. Read More