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David Chorney on Food and Drug Administration (FDA) | JD Supra
JD Supra· 7 hours agoThis Privacy Policy describes how JD Supra, LLC ("JD Supra" or "we," "us," or "our") collects, uses and shares personal data collected from visitors to ...
Soft drinks recall update as FDA sets risk level
Newsweek· 2 days agoThree soft drink products that were recalled by the Food and Drug Administration (FDA) for containing ...
FDA vaccine advisers vote unanimously in favor of updated Covid-19 shot for fall
CNN.com· 8 hours agoThe US Food and Drug Administration’s committee of independent advisers voted unanimously Wednesday...
MDMA drug for PTSD panned by FDA advisers citing trial flaws - The Boston Globe
The Boston Globe· 10 hours agoAdvisers to the Food and Drug Administration voted 9 to 2 that developer Lykos Therapeutics Inc.’s...
Salmonella linked to recalled cucumbers could be two separate strains; FDA, CDC investigate
USA Today· 10 hours agoThe Centers for Disease Control and Prevention and the Food and Drug Administration< ...
FDA Advisors Recommend Against Using MDMA for PTSD Treatment
Time via Yahoo News· 12 hours agoFood and Drug Administration (FDA) voted against adopting MDMA as a treatment for post-traumatic ...
US FDA warns on risks linked to sulfite-containing compounded drugs
Reuters· 8 hours agoThe U.S. Food and Drug Administration said on Wednesday it had alerted healthcare professionals, ...
Adults 60+ Will Have 3 RSV Vaccines to Choose From This Year
Verywell Health via Yahoo News· 9 hours agoThe FDA approved mRESVIA based on data from a clinical trial that included...any reactions to the...
Popular organic kids' snacks found to contain high levels of lead: Consumer Reports
AOL· 4 hours agoA study conducted by Consumer Reports discovered that two popular brands of kids' snacks contain elevated levels of lead, though federal standards have not been set on heavy metal levels in ...
FDA advisers overwhelmingly oppose approval of MDMA as a psychotherapeutic catalyst
Reason.com· 10 hours agoMembers...subjects, potential underreporting of adverse events, and allegedly inadequate assessment...
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