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Markets Herald W700Market Trends and Analysis • National Edition
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    Kazakhstan is Transitioning From Resource Extraction to Green Value Chains

    Kazakhstan is Transitioning From Resource Extraction to Green Value Chains

    Leveraging Data for Smarter Business Strategies With Insights From Shawn Dahl

    Leveraging Data for Smarter Business Strategies With Insights From Shawn Dahl

    Healthcare IT Decision Making Slowed by Economic Uncertainty, Survey Reveals

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FDA Approval

January 1, 2023

Congress Approves Landmark Measure to Reduce Animal Testing

May 1, 2022

FDA Approves Alexion’s Ultomiris for Treatment of gMG

November 13, 2021

FDA Approves Besremi to Treat Adults With Polycythemia Vera

The FDA granted the approval of Besremi to PharmaEssentia Corporation

July 1, 2021

FDA Approves Component of Treatment Regimen for Most Common Childhood Cancer

November 23, 2021

FDA Approves First Treatment for Common Type of Post-Transplant Infection That Is Resistant to Other Drugs

Approval is for cytomegalovirus, a type of herpes virus

October 8, 2021

FDA Approves Innovative Treatment for Pediatric Patients With Congenital Athymia

August 23, 2021

FDA Approves Pfizer-BioNTech COVID-19 Vaccine

May 18, 2022

FDA Authorizes First COVID-19 Test Available Without a Prescription That Also Detects Flu and RSV

September 1, 2022

FDA Authorizes Moderna, Pfizer-BioNTech Bivalent COVID-19 Vaccines for Use as a Booster Dose

February 13, 2022

FDA Authorizes New Monoclonal Antibody for Treatment of COVID-19 That Retains Activity Against Omicron Variant

June 7, 2021

FDA Grants Accelerated Approval for Alzheimer’s Drug Aduhelm

December 10, 2021

FDA Issues Improvement Plan Focused on Modernizing Foodborne Illness Outbreak Responses

The following is attributed to Frank Yiannas, FDA Deputy Commissioner for Food Policy and Response, and Stic Harris, D.V.M. director of the FDA's Coordinated Outbreak Response and Evaluation Network

September 29, 2022

FDA Modernization Act Passes U.S. Senate, Premised on Achieving Major Reduction in Animal Testing

FDA Takes Steps to Ensure Safety of Cinnamon Products Sold in the US
March 7, 2024

FDA Takes Steps to Ensure Safety of Cinnamon Products Sold in the US

May 1, 2024

FDA to Hold Listening Session as Part of Broader Work to Optimize Use of, and Processes for, Advisory Committees

July 9, 2024

FDA Updates Guidance to Further Empower Companies to Address the Spread of Misinformation

September 11, 2021

FDA Will Follow the Science on COVID-19 Vaccines for Young Children

October 6, 2021

Johnson & Johnson Submits Emergency Use Authorization Amendment to FDA to Support its COVID-19 Vaccine Booster

Novavax Headquarters. © Getty Images
November 11, 2024

Novavax Receives FDA Approval to Resume Phase 3 Trials for COVID-19-Influenza Vaccine Following Clinical Hold Lift

August 29, 2024

Precision Medicine Trailblazer Nuvectis Pharma Secures FDA Orphan Drug Designation for NXP800

The Orphan Drug Designation is more than just a regulatory milestone—it’s a strategic advantage that could dramatically reshape the future of Nuvectis Pharma.

April 10, 2022

Statement From FDA Commissioner Robert M. Califf, M.D., on Ensuring Access to Safe and Effective Treatments

Joint Statement with CMS Administrator Chiquita Brooks-LaSure

July 15, 2021

TransMedics Announces Positive FDA Advisory Committee Vote for the OCS Liver System

November 7, 2021

U.S. FDA Approves Nova Mentis Orphan Drug Application

September 6, 2022

U.S. Food and Drug Administration Awards $2.6 Million Orphan Products Development Grant

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Markets Herald W700Market Trends and Analysis • National Edition
  • Associated Press
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