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Human Drugs

Glycol Testing Guidance

FDA publishes an immediately-effective guidance to help drug manufacturers, repackers, and compounders prevent the use of glycol-contaminated glycerin...

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Federal Register

Info Collection on Expanded Access Form

Federal Register notice: FDA sends to OMB an information collection revision entitled Expanded Access to Investigational Drugs for Treatment Use.

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Human Drugs

CGMP Violations in Premier Nutra Pharma Inspection

FDA warns Carlsbad, CA-based Premier Nutra Pharma about CGMP violations in its work as a contract drug manufacturer.

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Human Drugs

Court Backs FDA in Somatuline Depot Case

The DC federal court says FDA is correctly regulating Ipsen Biopharmaceuticals Somatuline Depot as a drug rather than as a biologic as sought by the c...

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Medical Devices

FDA Clears Cumulus EEG Headset

FDA clears a Cumulus Neuroscience 510(k) for its dry-sensor Cumulus EEG headset and its use for the remote acquisition, display, and storage of electr...

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Human Drugs

Genentech Vabysmo sBLA for Macular Edema

FDA accepts for review a Genentech supplemental BLA for Vabysmo (faricimab-svoa) for treating macular edema following retinal vein occlusion.

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Human Drugs

Acrivon Gets 2 Fast Track Designations for Prexasertib

FDA grants Acrivon Therapeutics two fast track designations for developing ACR-368 (prexasertib) in platinum-resistant ovarian cancer and endometrial ...

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Medical Devices

AI/ML Predetermined Change Control Plan Guidance

Two Hyman, Phelps & McNamara attorneys and a medical device regulation expert analyze a recent FDA draft guidance on artificial intelligence/machine l...

Human Drugs

FDA OKs Expanded Farxiga Indication

FDA approves AstraZenecas Farxiga to reduce the risk of cardiovascular death, hospitalization for heart failure, and urgent heart failure visits in ad...

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Medical Devices

Cue Health Files De Novo App for RSV Test

Cue Health files a de novo submission seeking permission to market its Cue RSV Molecular Test for at-home and point-of-care use.