Why is "Food and Drug Administration" trending?

Search Interest Perspective

• US Food and Drug Administration Approves New Sunscreen Filter - The Business of Fashion
• Organon Secures US Food and Drug Administration Approval Expanding Indications for TOFIDENCE® (tocilizumab-bavi) in Cytokine Release Syndrome (CRS) and Pediatric COVID-19 - Stock Titan
• FSMA Final Rule on Requirements for Additional Traceability Records for Certain Foods - fda.gov
• FDA OKs first new sunscreen ingredient in more than 25 years - WRAL
• Honeywell Helps Deliver Resiliency and Cost Savings to Food and Drug Administration's White Oak Campus - Department of Energy (.gov)
• FDA alerts public to recall of packaged Dried Herring Fish - Spectrum News
• FDA expands sunscreen options with first new ingredient since 1990s - Reuters
• Critics call for National Priority Voucher program reform - C&EN
• Committee Approves FY27 Agriculture, Rural Development, Food and Drug Administration Act - House Committee on Appropriations (.gov)
• The US Food and Drug Administration approves the first new sunscreen ingredient in 20 years - صوت الإمارات
• New drug applications for Bayer’s FXIa inhibitor accepted by U.S. Food and Drug Administration under Priority Review and by Japan’s Ministry of Health, Labour and Welfare - Bayer
• Marty Makary out as head of US Food and Drug Administration - BBC
• FDA commissioner resigns after tumultuous tenure - NPR
• Outbreak Investigation of Infant Botulism: Infant Formula (November 2025) - fda.gov
• FDA conducting safety study of abortion drug mifepristone - Spectrum News
• The many ways FDA is responsible for protecting the public health. - fda.gov
• Digital Health Center of Excellence - fda.gov
• Food Allergies - fda.gov
• Talc - fda.gov
• Per- and Polyfluoroalkyl Substances (PFAS) - fda.gov
• Pierre Fabre Pharmaceuticals Announces Type A Meeting Agreed with U.S. Food and Drug Administration (FDA) for Tabelecleucel Biologic License Application (BLA) - PR Newswire
• BioPorto initiates U.S. Adult Validation Study following U.S. Food and Drug Administration (FDA) feedback - NTB Kommunikasjon
• The Food and Drug Administration’s Food Traceability Rule: Overview and Issues for Congress - Every CRS Report
• Pierre Fabre Pharmaceuticals Submits Type A Meeting Request to U.S. Food and Drug Administration (FDA) for Tabelecleucel Biologic License Application (BLA) - PR Newswire
• ACLU v. U.S. Food and Drug Administration - American Civil Liberties Union
• Donald Trump expected to fire head of Food and Drug Administration - Financial Times
• U.S. Food and Drug Administration Approves BioMarin's PALYNZIQ® (pegvaliase-pqpz) for Adolescents 12 Years of Age and Older with Phenylketonuria (PKU) - PR Newswire
• What does the Food and Drug Administration (FDA) do? - USAFacts
• Paws Off Xylitol; It's Dangerous for Dogs - fda.gov
• The latest COVID vaccines come with new FDA limits - NPR
• Diffusing authority to make drug approval decisions at the US Food and Drug Administration - Nature
• Head of the Food and Drug Administration resigns - WTVG
• US Food and Drug Administration Blocked Publication of Agency Studies Confirming Shingles and COVID-19 Vaccine Safety - Health Policy Watch
• FDA Commissioner canned; drug commercials continue - Raleigh News & Observer
• Reforms to modernize drug testing continue at Food and Drug Administration - Humane World for Animals
• Trump's FDA chief is out after angering pharma CEOs, vaping lobbyists and anti-abortion activists - AP News
• Trump says Marty Makary is out as Food and Drug Administration commissioner - Anadolu Ajansı
• Marty Makary out as FDA chief - Axios
• Why isn’t the Food and Drug Administration celebrating the decline in youth tobacco use? - Reason Foundation
• U.S. Food and Drug Administration Accepts for Priority Review Bristol Myers Squibb’s Supplemental New Drug Application for Camzyos (mavacamten) to Treat Adolescents with Symptomatic Obstructive Hypertrophic Cardiomyopathy (oHCM) - Business Wire
• Food and Drug Administration Expert Panel on Infant Formula “Operation Stork Speed” - American Society for Nutrition
• Head of the Food and Drug Administration resigns - FOX5 Vegas
• FDA reverses course on Moderna flu shot - NPR
• (tepotinib) to Identify Patients with MET Exon 14 Skipping Alterations in Non-Small Cell Lung Cancer - Business Wire
• Head of the Food and Drug Administration resigns - WIBW
• Deciphera Pharmaceuticals Announces U.S. Food and Drug Administration Acceptance for Filing of New Drug Application for Tirabrutinib in Patients with Relapsed or Refractory PCNSL - Business Wire
• FDA announces its first OK of fruit-flavored e-cig­a­rettes for adults in major shift under Trump - Spectrum News
• Head of the Food and Drug Administration resigns - WWBT
• Head of the Food and Drug Administration resigns - Hawaii News Now
• The FDA creates a quicker path for gene therapies - NPR
• Head of the Food and Drug Administration resigns - KY3
• FDA to Offer Bonus Payments to Staffers Who Complete Speedy Drug Reviews - WTTW News
• Head of the Food and Drug Administration resigns - WBTV
• Head of the Food and Drug Administration resigns - WSAW
• PIERRE FABRE PHARMACEUTICALS STATEMENT REGARDING RECEIPT OF COMPLETE RESPONSE LETTER FOR TABELECLEUCEL BIOLOGICS LICENSE APPLICATION FROM THE U.S. FOOD AND DRUG ADMINISTRATION - PR Newswire
• Head of the Food and Drug Administration resigns - AZ Family
• Head of the Food and Drug Administration resigns - KCTV
• Head of the Food and Drug Administration resigns - WSFA
• Trump administration's embattled FDA vaccine chief is leaving for the second time - NPR
• Makary out at FDA after facing pressure to resign - Roll Call
• Head of the Food and Drug Administration resigns - WRDW
• FDA moves toward easing restrictions on certain peptides - BioPharma Dive
• LivaNova Receives U.S. Food and Drug Administration Premarket Approval for aura6000 System to treat Moderate to Severe Obstructive Sleep Apnea - Yahoo Finance
• Head of the Food and Drug Administration resigns - WVLT
• Trump says Marty Makary is out as Food and Drug Administration head - AP News
• Overseeing Food and Drug Safety is Getting Harder at FDA - U.S. Government Accountability Office (.gov)
• FDA to raise hurdles for vaccines, faulting COVID shots for 10 kids' deaths - NPR
• Head of the Food and Drug Administration resigns - KXII
• Head of the Food and Drug Administration resigns - Atlanta News First
• Outlook Therapeutics Provides Regulatory Update on U.S. Food and Drug Administration Review of ONS-5010/LYTENAVA™ (bevacizumab-vikg) for the Treatment of Wet AMD - Yahoo Finance
• Head of the Food and Drug Administration resigns - KFDA | NewsChannel 10
• Head of the Food and Drug Administration resigns - WSAZ
• FDA warns of neurosurgical supply disruptions - Healthcare Dive
• FDA warns Novo Nordisk about side effect reporting vi­o­la­tions involving patients taking its GLP-1s - Spectrum News
• Head of the Food and Drug Administration resigns - KOLO | 8 News Now
• US FDA pushes for new methods to replace animal testing in early drug studies - Reuters
• Column: Makary is out, but the FDA is still far from normal - The Virginian-Pilot
• Head of the Food and Drug Administration resigns - KSLA
• Harmony Biosciences Receives U.S. Food and Drug Administration Approval for WAKIX - Business Wire
• US FDA approves first drug to delay heart failure in dogs - Reuters
• U.S. Food and Drug Administration (FDA) Accepts Teva’s New - GlobeNewswire
• U.S. Food and Drug Administration (FDA) Approves Updated Indication Statement for RINVOQ® (upadacitinib) for the Treatment of Inflammatory Bowel Disease - PR Newswire
• US FDA authorizes early access to Revolution's pancreatic cancer pill - Reuters
• FDA Will Drop Two-Study Requirement for New Drug Approvals, Aiming to Speed Access - WTTW News
• Marty Makary, Commissioner, Food and Drug Administration - The Presidential Prayer Team
• U.S. Food and Drug Administration (FDA) Accepts Teva’s New Drug Application (NDA) for Olanzapine Extended-Release Injectable Suspension (TEV-'749) for the Once-Monthly Treatment of Schizophrenia in Adults - Yahoo Finance
• Ascentage Pharma Announces IND Clearance by the U.S. Food and Drug Administration for BTK Degrader APG-3288 - Yahoo Finance
• U.S. Food and Drug Administration Accepts New Drug Application for Zipalertinib for the Treatment of Locally Advanced or Metastatic Non-Small Cell Lung Cancer with EGFR Exon 20 Insertion Mutations - Business Wire
• NRx Pharmaceuticals Announces US Food and Drug Administration (FDA) Receipt of ANDA for KETAFREE™, a Preservative-Free IV Ketamine - Yahoo Finance
• FDA Finds Little Evidence That Drug Touted by Trump Can Help People With Autism - WTTW News
• Corcept Therapeutics shares surge as lead drug gets FDA nod for ovarian cancer - Reuters
• U.S. Food and Drug Administration Accepts New Drug Application and Grants Priority Review for Takeda’s Oveporexton (TAK-861) as a Potential First-in-Class Therapy for Narcolepsy Type 1 - Business Wire
• FDA to start food sampling in mid-June for risk assessment - Global New Light Of Myanmar
• U.S. Food and Drug Administration Accepts Bristol Myers Squibb's New Drug Application for Iberdomide in Patients with Relapsed or Refractory Multiple Myeloma - Business Wire
• MEDIPOST Inc. Submits IND Amendment With U.S. Food and Drug Administration to Initiate Phase III Trial - BioSpace
• U.S. Food and Drug Administration Approves LIB Therapeutics’ LEROCHOL - Business Wire
• FDA Says Drugmakers Have Recalled Blood Pressure Medicine Tainted With a Cancer-Causing Chemical - WTTW News
• PureTech Announces Orphan Drug Designations Granted by the U.S. Food and Drug Administration and European Commission for Deupirfenidone (LYT-100) in Idiopathic Pulmonary Fibrosis - Business Wire
• FDA warning letter flags serious violations at New Jersey manufacturing facility for GLP-1 weight loss jabs - Cleanroom Technology
• ThinkTrends Agentic AI Goes Live With the U.S. Food and Drug Administration’s Nationwide Adverse Event Monitoring System - Business Wire