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FDA approves first self-test for cervical cancer
Homenewshere.com· 3 hours agoThe FDA now says self-collected vaginal samples can now be screened at doctor’s office or urgent care facilities.
Mizuho raises Sarepta Therapeutics stock target on FDA hopes By Investing.com
Investing.com· 52 minutes agoThis adjustment comes after a discussion with a former FDA regulatory clinical expert, which...
Critics Say FDA's Use of Surrogate Markers Falling Short
Medscape· 8 hours agoAs the FDA's use of surrogate endpoints in the drug approval process is increasing, researchers are...
FDA grants breakthrough therapy status for Nuvalent’s NVL-655
Pharmaceutical Technology via Yahoo Finance· 2 hours agoThe US Food and Drug Administration (FDA) has granted breakthrough therapy designation (BTD) for...
FDA approves self-collection screening tests for HPV, allowing women to avoid pelvic exams for...
FierceBiotech· 2 days agoThe FDA has approved two diagnostic devices that allow women to collect vaginal samples themselves...
FX Shoulder obtains FDA 510(k) clearance for glenoid baseplates
Medical Device Network via Yahoo Finance· 4 hours agoFX Shoulder Solutions has secured 510(k) clearance from the US Food and Drug Administration (FDA)...
Amgen’s IMDELLTRA receives FDA approval for lung cancer treatment
Pharmaceutical Technology via Yahoo Finance· 4 hours agoAmgen has announced the US Food and Drug Administration's (FDA) accelerated approval for its...
FDA greenlights self-collection of vaginal samples for cervical cancer screening
KMBC-TV Kansas City· 19 hours agoTwo health care businesses – biotechnology company Roche and medical technology firm Becton, Dickson...
FDA APPROVES IMDELLTRA™ (TARLATAMAB-DLLE), THE FIRST AND ONLY T-CELL ENGAGER THERAPY FOR THE...
FOX 5 San Diego· 14 hours agoAmgen (NASDAQ:AMGN) today announced that the U.S. Food and Drug Administration (FDA) has approved IMDELLTRA™ (tarlatamab-dlle) for the treatment of adult patients with extensive-stage ...
Why the U.S. is behind on sunscreen
USA TODAY via Yahoo News· 3 hours ago“We have asked the FDA to consider allowing market access.” The FDA is hamstrung by a 1938 law that requires sunscreens to be tested on animals and...
