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Human Drugs

J&J Responding to Coronavirus Crisis

Johnson & Johnson says its Janssen unit is cooperating with regulators, healthcare organizations, and others in a multi-pronged effort to respond to t...

Human Drugs

Hypertension Indication Labeling Guidance

FDA issues a guidance to help applicants develop labeling information demonstrating the connection between antihypertensive drugs and improved cardiov...

Human Drugs

Insulin Product Clinical Immunogenicity Guidance Comments

Stakeholders generally support the FDA position on clinical immunogenicity studies for biosimilar and interchangeable insulin products.

Human Drugs

CDER Proposing 80 Guidances in 2020

CDER issues a list of 80 new and revised draft guidances it plans to publish in 2020.

Human Drugs

FDA Revises Generic Drug Review Priority Policy

FDA revises the CDER MAPP dealing with the review of ANDAs, amendments, and supplements.

Human Drugs

FDA Denies Public Citizen Hetlioz Petition

FDA denies a Public Citizen petition seeking a narrower indication and labeling changes for Vanda's Hetlioz sleep disorder drug.

Medical Devices

Court Orders $344 Million in J&J Pelvic Mesh Case

The California Superior Court orders Johnson & Johnson to pay $343.99 million in penalties for false and deceptive marketing of its pelvic mesh produc...

Biologics

Deviations from HCT/P Regs Found at R&B Medical

FDA warns R&B Medical Group about HCT/P deviations in its work as a contract testing laboratory.

Federal Register

Voting Members Needed for CDRH Patient Panel

Federal Register notice: FDA requests nominations for voting members to serve on CDRHֺֺs Patient Engagement Advisory Committee.

Federal Register

16 Information Collections Cleared by OMB

Federal Register notice: FDA posts a list of 16 information collections approved by OMB.