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Human Drugs

FDA, Polynoma Agree on Study for Melanoma Vaccine

FDA and Polynoma reach agreement under a Special Protocol Assessment on a pivotal Phase 3 clinical trial of the companys melanoma cancer vaccine sevip...

Medical Devices

FDA Approves Cochlear Implants for Wider Deafness

FDA has approved a Cochlear Limited PMA for its Cochlear Nucleus Implants for treating unilateral hearing loss and single-sided deafness.

FDA General

Not the Time to Look at New Covid Approaches: Woodcock

FDA acting commissioner Janet Woodcock tells a Senate Health, Education, Labor & Pensions hearing that the current omicron variants effects on the hea...

Human Drugs

FDA OKs Idorsia Insomnia Drug

FDA approves an Idorsia Pharmaceuticals NDA for Quviviq (daridorexant) 25 mg and 50 mg for treating adult patients with insomnia.

Federal Register

Drug Supply Chain Security Info Collection

Federal Register notice: FDA sends to OMB an information collection revision entitled Drug Supply Chain Security Act Implementation (OMB Control Numbe...

Medical Devices

Guide on Device Supply Discontinuance/Interruption

FDA posts a draft guidance entitled Notifying FDA of a Permanent Discontinuance or Interruption in Manufacturing of a Device Under Section 506J of the...

Human Drugs

Allogene Therapeutics Clinical Hold Removed

FDA removes a clinical hold on Allogene Therapeutics AlloCAR T clinical trials after a chromosomal abnormality was determined to be unrelated to the t...

Medical Devices

Cardiovascular Systems Recall Wirion Device

Cardiovascular Systems recalls its Wirion system due to complaints about filter breakage during retrieval.

Human Drugs

Fast Track for Retinal Therapy

FDA grants 4D Molecular Therapeutics a fast track designation for 4D-125 for treating patients with inherited retinal dystrophies due to defects in th...

Federal Register

Latest Federal Register Notices

FDA Review posts the Federal Register notices for the week ending 1/7/2022.