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Ro's Supply Tracker Helps Patients Locate In-Demand GLP-1 Drugs Amid Shortages
⏲ 0:35 👁 395K
What The FDA's Approval Of Aducanumab Might Mean For A BOOMING Clinical Research Industry!
⏲ 7 minutes 15 seconds 👁 95
FDA NanoDay Symposium 2022 Welcome, Keynote and Session 1
⏲ 1 hour 43 minutes 9 seconds 👁 937
AWANI Tonight: Synthetic nicotine in vapes may be more potent than nicotine, FDA finds
⏲ 1:12 👁 20K
About FDA’s Biomarker Qualification Program
⏲ 2 minutes 29 seconds 👁 26K
FDA NanoDay Symposium 2022 Session 2
⏲ 1 hour 16 minutes 4 seconds 👁 606
FDA Pulls Infant Formula from Shelves Due to Lack of Evaluation
⏲ 0:29 👁 285K
Petrie-Flom Center | Assessing the Viability of FDA’s Biosimilar Pathway
⏲ 1 hour 24 minutes 3 seconds 👁 150
FDA Perspectives on Biosimilar BLA-Manufacturing (28of33) Quality – Oct. 16-17, 2019
⏲ 24 minutes 48 seconds 👁 998
Origins of Dantrium® IV, Part 12: FDA Approval
⏲ 6 minutes 37 seconds 👁 61
FDA Guidance on Biosimilars
⏲ 8 minutes 8 seconds 👁 341
FDA Approval of the PFIZER Vaccine
⏲ 1 minute 30 seconds 👁 38
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_ro39s-supply-tracker-helps-patients-locate-in-demand-glp-1-drugs-amid-shortages.webp "Telehealth company Ro launched a new online tracker to help patients find popular weight loss and diabetes drugs called GLP-1s. These drugs have faced shortages in the US. Demand has outpaced manufacturers' ability to scale up production. Ro's Supply Tracker provides real-time data on drug availability, dose size, and pharmacy location to help more people access treatments. Notifications help users find pharmacies with supplies and request prescription transfers. The data may also help the FDA keep shortage lists updated."){kind=tracking}
_what-the-fda39s-approval-of-aducanumab-might-mean-for-a-booming-clinical-research-industry.webp "Dan Sfera")
_fda-nanoday-symposium-2022-welcome-keynote-and-session-1.webp "U.S. Food and Drug Administration")
_awani-tonight-synthetic-nicotine-in-vapes-may-be-more-potent-than-nicotine-fda-finds.webp "Nicotine alternatives in vapes may be more potent and addictive than nicotine itself, according to research by the US Food and Drug Administration and independent researchers.")
_about-fdas-biomarker-qualification-program.webp "U.S. Food and Drug Administration")
_fda-nanoday-symposium-2022-session-2.webp "U.S. Food and Drug Administration")
_fda-pulls-infant-formula-from-shelves-due-to-lack-of-evaluation.webp "Crecelac and Farmalac-branded infant formula is being recalled after being placed on shelves without proper evaluation by the Food and Drug Administration. According to the FDA, the products \")
_petrie-flom-center-124-assessing-the-viability-of-fdas-biosimilar-pathway.webp "Harvard Law School")
_fda-perspectives-on-biosimilar-bla-manufacturing-28of33-quality-oct-16-17-2019.webp "U.S. Food and Drug Administration")
_origins-of-dantrium-iv-part-12-fda-approval.webp "MHAUSvideo")
_fda-guidance-on-biosimilars.webp "PPD")
_fda-approval-of-the-pfizer-vaccine.webp "Borland Groover")
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