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The Management Committee may designate a limited number of Official Observers to the Management Committee from the World Health Organization and other regulatory authorities on the basis of perceived contribution or value to IMDRF. Official Observers do not participate in the decision making process. Official Observers must be approved by the unanimous consent of the Management Committee and, as with Members, need to be fully knowledgeable on IMDRF matters.
- Argentina, National Administration of Drugs, Food and Medical Devices
- World Health Organization (WHO)
- Saudi Food and Drug Authority
- Swissmedic
IMDRF Official Observer Representatives
Argentina - National Administration of Drugs, Food and Medical Devices (ANMAT)
- Lorena Terrizzano
Alternate National Director of the National Institute of Medical Devices (INPM)
National Administration of Drugs, Food and Medical Devices (ANMAT)
Email:lorena.terrizzano [at] anmat.gob.ar ( lorena[dot]terrizzano[at]anmat[dot]gob[dot]ar) - Rodrigo Pineiro
Director of the Office of the Institutional Relations
National Administration of Drugs, Food and Medical Devices (ANMAT)
Email: rodrigo.pineiro [at] anmat.gob.ar (rodrigo[dot]pineiro[at]anmat[dot]gob[dot]ar)
World Health Organization (WHO)
- Mr Hiiti Sillo
Unit Head, Regulation and Safety
World Health Organisation (WHO)
Email: silloh [at] who.int (silloh[at]who[dot]int) - Ms Irena Prat
Team Lead, In Vitro Diagnostic Assessment
World Health Organisation (WHO)
Email: prati [at] who.int (prati[at]who[dot]int)
Saudi Arabia - Saudi Food and Drug Authority
Switzerland - Swissmedic
- Mr Markus Wälti
Head of Division
Division Medical Devices Vigilance
Swiss Agency for Therapeutic Products
Email: Markus.waelti [at] swissmedic.ch (Markus[dot]waelti[at]swissmedic[dot]ch) - Mr Andre Breisinger
Market Surveillance
Expert Medical Devices Regulation
Swiss Agency for Therapeutic Products
Email: andre.breisinger [at] swissmedic.ch (andre[dot]breisinger[at]swissmedic[dot]ch)