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Human Drugs

Gemini Therapeutics Fast Track for Macular Degeneration Drug

FDA grants Gemini Therapeutics a fast track designation for GEM103, an investigational treatment for dry, age-related macular degeneration.

Federal Register

FDA Debars Insys Sales Manager

Federal Register notice: FDA issues an order to permanently debar former Insys Therapeutics regional sales manager Joseph A. Rowan.

Federal Register

Insys Therapeutics Sales Manager Debarred

Federal Register notice: FDA issues an order to permanently debar former Insys Therapeutics regional sales manager Sunrise Lee.

Human Drugs

RedHill Bio Fast Track for Antibacterial

FDA grants RedHill Biopharma a fast track designation for RHB-204 and its use as a potential first-line, stand-alone, oral treatment for pulmonary non...

Medical Devices

Brain Therapy for Alzheimers Breakthrough Status

FDA grants Functional Neuromodulation a breakthrough device designation for the Vercise Deep Brain Stimulation System for treating patients 65 years a...

Medical Devices

Tidepool 510(k) for iPhone Insulin Dosing App

Tidepool files a 510(k) for an automated insulin dosing app for use on the iPhone for managing Type 1 diabetes.

Medical Devices

FDA Joining Pathology Innovation Collaborative Community

MDIC says FDA is joining its new Pathology Innovation Collaborative Community.

Federal Register

Guide on Device Safer Technologies Program

Federal Register notice: FDA makes available a final guidance entitled Safer Technologies Program for Medical Devices.

Federal Register

Gene Therapy for Neurodegenerative Diseases Guidance

Federal Register notice: FDA makes available a draft guidance entitled Human Gene Therapy for Neurodegenerative Diseases.

Human Drugs

Teva Raises BA/BE Retention Sample Compliance Policy Concerns

Teva raises concerns with an FDA compliance policy on bioavailability and bioequivalence samples to be retained.