FDA requires more postmarket data to keep certain devices on the market
September 16, 2019
Medical Design & Outsourcing has published an article regarding FDA’s recent announcement require Medical Device manufacturers to provide more Real World Evidence for certain premarket approvals or risk losing those approvals.
To read the entire article, click the button below.
Discover What Sets TrialStat Apart From Ordinary EDC Platforms
Click the image or button below to explore our eClinical Suite Platform and discover what sets TrialStat apart from competing EDC platforms.
Request Your Demo Today!
From rapid database build through database lock, we deliver consistent quality on-time and on-budget. Ready to upgrade your eClinical toolkit?