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12K views · 23 reactions | Dr. Peter Marks, director of the Center for Biologics Evaluation and Research at the U.S. Food and Drug Administration, discusses the manufacturing process and potential risks associated with CAR T-cell therapy. Gain a deeper understanding of the complexities surrounding this innovative treatment on Intention to Treat: https://nej.md/itt-ep29 | The New England Journal of Medicine | Facebook
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12K views · 23 reactions | Dr. Peter Marks, director of the Center for B…
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Dr. Peter Marks, former director of the FDA’s Center for Biologics Evaluation and Research, has been a staunch advocate for the safety and efficacy of vaccines approved in the United States. He emphasized that vaccines undergoing the FDA’s rigorous approval process are of high quality, stating, “No one at FDA would ever let a vaccine out that they would not give to their own children.” Dr. Marks highlighted the measles vaccine as one of the safest and most effective, noting that it has saved an
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MEDICAL WATCH: Lutathera is a radioactive cancer drug made in Italy that was just approved by the FDA. The CHI Theranostics Center is the first in the state to import the drug. The doctor in charge says it's the future of cancer treatment. MORE: http://www.ketv.com/article/italian-radioactive-cancer-drug-comes-to-nebraska/18658982 | Erin Hassanzadeh
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1.9K views · 18 shares | Ever wonder what it takes to take a drug from discovery to market? Dr. Theresa Strong discusses the stages of development and how you can help not only get drugs through clinical trials but also with the approval process. You can watch the entire presentation that includes information on each clinical trial here: https://www.fpwr.org/blog/2019-pws-clinical-trials-panel-video | The Foundation for Prader-Willi Research | Facebook
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1.9K views · 18 shares | Ever wonder what it takes to take a drug from d…
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Exclusive | Children with autism are showing ‘dramatic improvement’ with this cheap drug — and doctor behind its research says it may one day prevent the disorder
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