Office of the Commissioner

Articles by Office of the Commissioner

FDA Takes New Approach to "No Artificial Colors" Claims - fda.gov

Business February 7, 2026

For Immediate Release: February 05, 2026 Today, the U.S. Food and Drug Administration took additional steps to support the transition of our nations food supply from the use of artificial petroleum�...

FDA Increases Flexibility on Requirements for Cell and Gene Therapies to Advance Innovation - fda.gov

Business January 13, 2026

For Immediate Release: January 11, 2026 The U.S. Food and Drug Administration today announced it is sharing information about the agencys flexible approach to overseeing chemistry, manufacturing an�...

FDA Eliminates Major Barrier to Using Real-World Evidence in Drug and Device Application Reviews - fda.gov

Business December 16, 2025

For Immediate Release: December 15, 2025 The U.S. Food and Drug Administration (FDA) today removed a key limitation on the use of real-world evidence (RWE) used in drug and device applications revi�...

FDA Approves Two Oral Therapies to Treat Gonorrhea - fda.gov

Business December 13, 2025

For Immediate Release: December 12, 2025 The U.S. Food and Drug Administration recently approved two new oral medicines to treat a common sexually transmitted infection called gonorrhea. The FDA t�...

FDA Proposes Expanding Sunscreen Active Ingredient List - fda.gov

Business December 12, 2025

For Immediate Release: December 11, 2025 Today, the U.S. Food and Drug Administration announced that it is taking action to advance sunscreen innovation, part of a broader initiative in the Office �...

First Approval in Commissioner's National Priority Voucher Pilot Program Strengthens Domestic Antibiotic Manufacturing Capacity - fda.gov

Business December 11, 2025

For Immediate Release: December 09, 2025 The U.S. Food and Drug Administration today approved Augmentin XR (amoxicillin-clavulanate potassium) under the Commissioner's National Priority Voucher (CN�...

FDA Approves First CAR T-Cell Therapy for Marginal Zone Lymphoma In the US - fda.gov

Business December 6, 2025

For Immediate Release: December 04, 2025 The U.S. Food and Drug Administration today approved a new indication for Breyanzi (Lisocabtagene maraleucel) as the first Chimeric Antigen Receptor (CAR) T�...