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Medical Devices

Medical Device Safer Technologies Program Guidance

FDA issues a guidance with an overview of the new Safer Technologies Program for some medical devices and device-led combination products.

Federal Register

FDA Debars Former Insys Sales Manager

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

Federal Register

Drug Distributor Owner Debarred by FDA

Federal Register notice: FDA issues an order to permanently debarring former Cumberland Distribution owner Jerrod Nichols Smith from providing service...

Federal Register

Guide on INDs for Antisense Oligonucleotide Drugs

Federal Register notice: FDA makes available a draft guidance entitled IND Submissions for Individualized Antisense Oligonucleotide Drug Products: Adm...

Human Drugs

Nostrum Labs Recalls Metformin Lot

Nostrum Laboratories recalls one lot of metformin HCl extended release tablets after it was determined to contain levels of nitrosamine impurities abo...

Human Drugs

Stokes Healthcare FDA-483

FDA releases an FDA-483 with four observations from an inspection at the Stokes Healthcare outsourcing facility.

Human Drugs

Advancing New Alternative Methodologies Report

FDA issues a report on steps it has taken to integrate alternative approaches into regulatory programs.

Federal Register

Mouse Embryo Assay for Reproduction Tech Devices Guide

Federal Register notice: FDA posts final guidance entitled Mouse Embryo Assay for Assisted Reproduction Technology Devices.

Medical Devices

Alert on Covid Test False Negatives

FDA issues a safety alert about false negatives with KorvaLabs Curative SARS-Cov-2 (Covid-19) test.

Biologics

No Evidence Supporting Covid Vaccine Dosing Changes: FDA

FDA commissioner Stephen Hahn and CBER director Peter Marks strongly urge healthcare providers not to unilaterally alter the FDA-authorized dosing sch...