Name
Session 1: Regulatory Updates from IMDRF Management Committee and Official Observers (Continued)
Date & Time
Tuesday, March 12, 2024, 11:00 AM - 11:50 AM
Speakers
Dr. Laura Squire, Chief Healthcare Quality and Access Officer, MHRA
Ms. Melissa Torres, Associate Director for International Affairs, U.S. FDA
Mariela Aranda, Head of IVD Departament, ANMAT Argentina
Mr. André Breisinger, Medical Devices Regulation Expert, Swissmedic
Ms. Irena Prat, Team Lead, World Health Organization
Laura Squire Mariela Aranda André Breisinger Irena Prat
Description

United Kingdom

  • Laura Squire, Chief Healthcare Quality and Access Officer, MHRA

11:00 to 11:10 AM

United States of America 

  • Melissa Torres, Associate Director for International Affairs, U.S. FDA

11:10 AM to 11:20 AM

Argentina (Official Observer)

  • Mariela Aranda, Head of the Service of In Vitro Diagnostic Products, ANMAT 

11:20 to 11:30 AM

Switzerland (Official Observer)

  • André Breisinger, Expert Medical Devices Regulation, Medical Devices Surveillance, Swissmedic

11:30 to 11:40 AM

World Health Organization (Official Observer)

  • Irena Prat, Team Lead, In Vitro Diagnostics Assessment, Prequalification Unit, WHO

11:40 to 11:50 AM
Location Name
Amphitheater
Full Address
Ronald Reagan Building & International Trade Center
1300 PENNSYLVANIA AVENUE NW
Washington, DC 20004
United States
Session Type
General Session