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...On Wednesday the General Court upheld the decision, saying the trademark would be associated “with drug trafficking and narco-terrorism and with the crimes and suffering resulting therefrom”....
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...A decision on Eli Lilly’s donanemab drug from the US Food and Drug Administration was originally due by the end of the first quarter, but the medicine will now be subject to a further review by an advisory...
...The first mental health treatment using schedule-1 drug MDMA faces a significant regulatory hurdle as the US Food and Drug Administration is poised to ask outside experts to scrutinise the treatment for...
...These will be the first results from a study designed around landmark US Food and Drug Administration guidelines for researching psychedelics that were outlined last year, a decision that encouraged investors...
...According to a Food and Drug Administration database tracking drug shortages, lower doses of Wegovy have limited availability at present but higher doses and Ozempic injections are in good supply....
...to a US Food and Drug Administration database tracking shortages....
...But the administration hasn’t stopped there....
...A Humira biosimilar from Teva Pharmaceuticals working with Alvotech earlier this year became the first drug that the US Food and Drug Administration granted interchangeable status, which lets pharmacists...
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...The US Food and Drug Administration originally planned to have concluded the approval decision for Moderna’s respiratory syncytial virus vaccine by May 12 but the decision has been delayed to the end of...
...MainFT: Joe Biden’s administration is planning to reclassify cannabis as a less harmful drug with a smaller legal penalty, in a historic shift for US drug policy, said people familiar with the matter....
...Drug Enforcement Administration, said the Chapitos had “pioneered the manufacture and trafficking of fentanyl” and “flooded” the US with the drug....
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...The antitrust regulator wrote to 10 pharmaceutical manufacturers to inform them the agency had disputed their patents with the Food and Drug Administration, giving the companies a 30-day window to respond...
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