Smug Fvcking Psychopath
Another UNQUALIFIED, Bootlicking QANON Lunatic
Republican War On Women
UnAmerican
Unconstitutional
Misogyny
Sharia Law

Smug Fvcking Psychopath
Another UNQUALIFIED, Bootlicking QANON Lunatic
Republican War On Women
UnAmerican
Unconstitutional
Misogyny
Sharia Law
#FDA Panel Backs #Galleri Multi-Cancer Early Detection Test - www.disabled-world.com/medical/phar...
The FDA has elevated a nationwide thyroid medication recall to Class I, its highest risk classification, after tablets from Vitruvias Therapeutics were found to be "superpotent." πβ οΈ
Synthetic #ThyroidMedicine R either contaminated or subpotent. #JoeBidenβs #FDA blocked importation from companies but
#IgnorantConvictedCorruptPedoRapistVulgarian #DonaldTrump lifted Bidenβs ban & now PPL R sick from #FDAApprovedMedicines
All who voted 4 #ignoramosIlliterateidiotInWH voted 4 this!
#FDA is looking to add more flexibility for companies to get more #vapes and tobacco pouches authorized, sources said. (Gift article)
www.wsj.com/politics/pol...
his recommendation and overview on vaccination guidelines. That was an extremely tough vaccination drive to conduct when normal americans were ragging and showing anger from unchecked and unverified vaccination conspiracy theories.
#FDA #Vaccination #VaccineBoosterShots
#VaccinationProgrammes
The only problem is that it's not too accurate, according to big studies. But they have friends at the FDA so it doesn't make a difference, right? www.wsj.com/health/healt... #grail #fda
#administration #cancer #early detection #FDA #Hong Kong
π www.newsmart.ch
Securities Class Action Filed Against Replimune Group, Inc. with Deadline Approaching #Class_Action #FDA # #Replimune_Group
Glytec's Glucommander Pediatrics Gains FDA Breakthrough Device Status for Infant Insulin Management #USA #Atlanta #FDA #Glytec #Glucommander
The #FDA has approved #EliLilly's once-weekly #basalinsulin product #Onswik for adults with #type2diabetes, setting up a market tussle with Novo over its recently launched Awiqli.
𧬠The #FDA has granted Fast Track and Orphan Drug designations to apitegromab for FSHD as dosing begins in the phase 2 FORGE trial.
The study will assess:
πΉ ~60 adults
πΉ 52 weeks of treatment
πΉ MRI-measured lean muscle volume
π Read more: www.neurologylive.com/view/fda-gra...
#FSHD #Neurology
WuXi Biologics Reinforces Quality and Reliability with Successful FDA GMP Inspection #China #FDA #Wuxi #WuXi_Biologics #GMP_Inspection
π #FDA Drug Approvals β September 2026
#Lirafugratinib, #Isembyld & #Zanvastro bring new approaches targeting FGFR, myostatin & RNA.
#Sevabertinib, #Camizestrant, #Imlunestrant, #Aqneursa & #Joenja expand therapeutic options across cancer, rare diseases & genetic disorders.
The good news for #Grail is that the #FDA's panel of external experts voted in favour of its #Galleritest for multiple cancers at a meeting yesterday. The bad news is that the discussions revealed some had misgivings about the #bloodtest β even if they voted for it.