Webinar Monitoring substandard and falsified medical devices

Webinar Monitoring substandard and falsified medical devices
Webinar Monitoring substandard and falsified medical devices

The Pan American Health Organization and the World Health Organization (WHO), is pleased to invite you to the Webinar Monitoring substandard and falsified medical devices with the objetive to discuss the monitoring of substandard and falsified medical devices based on the global experiences of the WHO and the national experiences of the regulatory agencies CECMED/Cuba and ANVISA/Brazil.

How to join

Agenda

Time EDT

Topic

Responsible

10:00 – 10:05

Opening and Welcome

PAHO

10:05 – 10:20

Experience in monitoring substandard and falsified medical devices

CECMED (Cuba)

10:20 – 10:35

Experience in monitoring substandard and falsified medical devices

Anvisa (Brazil)

10:35 – 10:45

Presentation of the results of the consultation to the countries of the region of the Americas on the regulation of substandard and falsified medical devices

PAHO

10:45 – 11:05

Global activities related to substandard and falsified medical devices

WHO

11:05 – 11:25

Questions and answers

All participants

11:25 – 11:30

Closing

PAHO

 Time correspondence

• 7:00 a.m. – Los Angeles, Vancouver

• 8:00 a.m. – Belmopan, Guatemala City, Managua, Mexico City, San Jose (CR), San Salvador, Tegucigalpa

• 9:00 a.m. – Bogota, Panama City, Kingston, Lima, Quito, Cayman Islands

• 10:00 a.m. – Asuncion, Bridgetown, Caracas, Castries, Georgetown, Havana, La Paz, Nassau, Ottawa, Port-au-Prince, Port of Spain, San Juan, Santiago, Santo Domingo, Washington DC

• 11:00 a.m. – Buenos Aires, Brasilia, Montevideo, Paramaribo

• 4:00 p.m. – Geneva, Madrid, Barcelona

For other cities, check the local time in the following link