Name
Next Steps
Date & Time
Monday, March 11, 2024, 4:10 PM - 4:50 PM
Speakers
Augusto Geyer, Regulatory Specialist, Office of Medical Devices, ANVISA
Mr. Markus Wälti, Head of Division Medical Devices Vigilance, Swissmedic
Ms. Maria Cecilia Lopez Gutierrez, Head of Medical Devices Registration Office, ISP, Chile
Ms. Paulyne Wairimu Dr., Head of Medical Devices & IVDs, Pharmacy & Poisons Board, Kenya
Nicole Taylor Smith, Vice President, Head of Regulatory Science & Policy, Philips
Fatemeh Razjouyan, Director, Regulatory Policy, International and Harmonization, Medtronic
Mr. Jesus Rueda Rodriguez, Director General International Affairs, MedTech Europe
Dr. Elaine Grimes, Devices Regulatory Specialist, MHRA
Augusto Geyer Markus Wälti Maria Cecilia Lopez Gutierrez Paulyne Wairimu Nicole Taylor Smith Fatemeh Razjouyan Jesus Rueda Rodriguez Elaine Grimes
Description

Panel Discussion  

  • Augusto Geyer, Head of Medical Devices Office, ANVISA
  • Markus Wälti, Head of Division Medical Devices Vigilance in Medical Devices Surveillance, Swissmedic, Swiss Agency for Therapeutic Products 
  • Maria Cecilia López, Head of Medical Devices Registration Subdepartment, ISP, Chile
  • Paulyne Wairimu, Medical Devices and Diagnostics Lead, Pharmacy and Poisons Board, Kenya; Chair, African Medical Devices Forum
  • Nicole Taylor Smith, Global Head of Regulatory Science and Policy, Philips
  • Fatemeh Razjouyan, Director of Regulatory Policy, International and Harmonization, Medtronic
  • Eve Hutchinson, Head of Regulation in the Innovative Devices team, MHRA
  • Jesús Rueda Rodríguez, Director General Strategies, Special Projects and International Affairs, MedTech Europe

4:10-4:50 PM
Location Name
Amphitheater
Full Address
Ronald Reagan Building & International Trade Center
1300 PENNSYLVANIA AVENUE NW
Washington, DC 20004
United States
Session Type
General Session