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Human Drugs

FDA Refuses to File NurOwn BLA

FDA refuses to file a BrainStorm Cell Therapeutics BLA for its NurOwn to treat ALS.

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Medical Devices

Strengthen AI Product Approval: Researchers

Yale University researchers say FDA should strengthen its regulatory approach to artificial intelligence products used in breast cancer screening.

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Federal Register

Draft Guide on ANDA Sameness Evaluations

Federal Register notice: FDA makes available a draft guidance entitled Sameness Evaluations in an ANDA Active Ingredients.

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Human Drugs

Panel Backs AstraZeneca Asthma Product in Adults

FDAs Pulmonary-Allergy Drugs Advisory Committee votes 16 to 1 to support approval of an AstraZeneca NDA for PT027 (albuterol/budesonide) for treating ...

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Marketing

ZoomRx Keys to Better Oncology Promo Messaging

ZoomRx suggests three ways to create effective oncology promotional messages directed to healthcare providers.

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Medical Devices

Insulet Diabetes Manager Correction

FDA says Insulet has issued a correction for its Omnipod DASH personal diabetes managers due to issues with the batteries.

Human Drugs

EUA for Kineret to Treat Covid-19 in Some Adults

FDA grants an emergency use authorization to Swedish Orphan Biovitrum for its Kineret to treat some adults hospitalized with Covid-19.

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Federal Register

FDA Cancels Panel Meeting on GSKs Zejula

Federal Register notice: FDA cancels an 11/22 Oncologic Drugs Advisory Committee meeting to discuss a GlaxoSmithKline supplemental NDA for Zejula (nir...

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Human Drugs

18 Observations on Lupin FDA-483

FDA releases the form FDA-483 issued following an inspection at the Lupin manufacturing facility in Pune, Maharashtra, India.

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Human Drugs

ImprimisRx NJ FDA-483 Has 9 Observations

FDA releases the form FDA-483 issued following an inspection at Ledgewood, NJ-based Imprimis Rx NJ.