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FDA approves Imdelltra for patients with extensive-stage small cell lung cancer
United Press International via Yahoo News· 2 hours agoImportantly, tarlatamab (Imdelltra) is only for patients who have exhausted all other options to...
The FDA's New Pre-Harvest Agricultural Water Rule: Impacts on PFAS-Contaminated Groundwater? | JD...
JD Supra· 30 minutes agoWith certain exceptions for growers of Covered Produce, the FDA's new rule requires pre-harvest agricultural water assessments for hazard identification and risk management ...
FDA-Approved HPV Self-Screening Tests Aim to Improve Cervical Cancer Prevention
Verywell Health via Yahoo News· 3 hours agoLalocracio / Getty Images Fact checked by Nick Blackmer Key Takeaways The FDA has approved a new...
Brainomix swings FDA clearance for its lung imaging AI software
Medical Device Network via Yahoo Finance· 6 hours agoThe FDA clearance follows a phase II clinical trial which found the Brainomix 360 e-Lung system...
Analysts weigh in on FDA's approval for Amgen's small cell cancer drug By Investing.com
Investing.com· 5 hours agoThe U.S. Food and Drug Administration (FDA) on Thursday granted accelerated approval to Amgen's...
Popular immune support tea bags recalled over possible pesticide contamination
Scripps News via AOL· 2 hours agoFood and Drug Administration. The recall applies to bags of the popular organic Yogi Echinacea...
BD's (BDX) FDA-Approved Test to Offer Wider Testing Access
Zacks via Yahoo Finance· 3 hours agoBD's (BDX) receipt of the FDA's clearance for the use of self-collected vaginal specimens for HPV...
Critics Say FDA's Use of Surrogate Markers Falling Short
Medscape· 14 hours agoAs the FDA's use of surrogate endpoints in the drug approval process is increasing, researchers are...
FDA leaders talk adcomms, shortages
Politico· 3 hours agoWith help from Ben Leonard FDLI ROUNDUP — Senior FDA officials gave a series of mini-updates on policy and agency issues ahead of the anticipated election-season slowdown ...
FDA grants breakthrough therapy status for Nuvalent’s NVL-655
Pharmaceutical Technology via Yahoo Finance· 9 hours agoThe US Food and Drug Administration (FDA) has granted breakthrough therapy designation (BTD) for...
