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Human Drugs

FDA Conducts 3 Inspections at CRO BioPharma Services

FDA completes three inspections this month at contract research organization BioPharma Services without issuing any Form 483s.

Medical Devices

Killed by FDA-approved Device: Amy Reed Dies of Cancer

Anti-morcellation pioneer Amy Reed dies of her cancer.

Human Drugs

Complete Response for Sun Elepsia XR

FDA tells Sun Pharma its Elepsia XR NDA cannot be approved until inspection deficiencies at the firms Halol facility are resolved.

Human Drugs

FDA Gives eCTD Master File Instructions

An FDA small business assistance podcast gives steps involved in meeting the requirement to electronically submit master files and associated document...

Human Drugs

Reps Want Office-Use Drug Compounding

Sixty-five House members urge FDA to rescind a guidance banning physician office-use drug compounding.

Human Drugs

ODAC Backs Emmaus Endari

The FDA Oncologic Drugs Advisory Committee votes to recommend to the agency that the risk/benefit profile for Emmaus sickle cell disease drug Endari i...

FDA General

Budget Hearing Rebuffs Trump Bid to Hike FDA User Fees

During FDA Commissioner Scott Gottliebs first Hill visit, House budget lawmakers dismiss the Trump Administrations request to renegotiate user fee agr...

Human Drugs

Orphan Status for Abeona Therapeutics Gene Therapy

FDA grants Abeona Therapeutics an Orphan Drug Designation for its EB-101 gene therapy program for patients with dystrophic epidermolysis bullosa.

Federal Register

OMB Approves Several Information Collections

Federal Register notice: FDA publishes a list of information collections that have been approved by the Office of Management and Budget.