Vee (Vasiliki) REVITHI is a Chemist/PhD in Biochemistry, and has worked for 36 years in EOF, the Medicines Authority of Greece. She has been a Head of Division for more than 15 years, 10 of them as Head of the GMDP Inspectorate of the Agency.

 

Vee led the implementation of a Quality System according to EU, PIC/S and ISO 17020 requirements in the Greek GMDP Inspectorate, the relevant Inspections methodology and the accession of EOF to PIC/S in 2002. She has been involved in the preparation of many regulations regarding medicines and medical devices, in a national and EU level.

She has participated for more than 25 years in EU meetings in Brussels and in the EMA in London.

 

Vee represented EOF/Greece in the PIC/S Committee (2002 to 2013) and has been a member of its Executive Bureau, more specifically she has been the Chair of Compliance Group (monitoring new applications at PIC/S). She was involved in several Inspectorates’ PIC/S and EU assessment Teams (US FDA, Romania, Austria, Cyprus, Iran, Uganda, Armenia, UNICEF) and was involved at the EU-Japan MRA in 2002-2003.

 

She performed GMP inspections in cooperation with EDQM and WHO Prequalification Program in India and China and participated in missions of the “Assistance to CFDA” project by WHO/Global Fund (2010 - 2013).

 

She worked for Roche, Switzerland (June 2013 to May 2018) in External Relations Europe, taking part in several International Conferences (ISPE, PDA etc)

 

Due to her long experience in PIC/S and EU regulations on GMDP, she has been providing consultancy to Authorities for their accession to PIC/S, eg. Armenia, Turkey, Jordan. She has been cooperating with the Gates Foundation Project for Technical Assistance to CFDI China for their preparation towards accession to PIC/S.