
@ShahidNShah
WASHINGTON, D.C. – A new report published in JAMA (Journal Against Medical Advice) found the Food and Drug Administration’s plan to streamline the process of approving drugs has been made possible by removing the cumbersome step of reviewing any and all pertinent evidence.
“When we stepped back and asked what was the biggest hurdle in the FDA’s process of approving of new drugs for the market we found that reviewing clinical trials and their evidence as the major rate-limiting step,” explained FDA spokesperson Ira Brisk. “Over the past few decades, we have made good progress rolling out novel drugs based on weaker evidence. It’s time to take the next step forward. Evidence shmevidence.”
Continue reading at gomerblog.com
Consider your most recent healthcare interaction. It likely involved some sort of medical device or equipment — a blood pressure monitor, a continuous glucose monitor, maybe even an MRI scanner. This …
Posted Jan 17, 2020iot
Connecting innovation decision makers to authoritative information, institutions, people and insights.
Medigy accurately delivers healthcare and technology information, news and insight from around the world.
Medigy surfaces the world's best crowdsourced health tech offerings with social interactions and peer reviews.
© 2025 Netspective Foundation, Inc. All Rights Reserved.
Built on Mar 13, 2025 at 4:03am