Group

Hatice Erkan

Chair of the Regulatory Affairs & Quality Working Group,
Senior Regulatory Affairs and Pharmacovigilance Specialist, Monrol Europe
BSc. Pharmacy, MSc. Biochemistry.
More than 10 years of experience in Regulatory Affairs and Pharmacovigilance and more than 3 years of experience in Global Regulatory Affairs of radiopharmaceuticals.

Cristiana Gameiro

Vice-Chair of the Regulatory Affairs & Quality Working Group
Product manager
IBA RadioPharma Solutions

Ger Mannie

Head Regulatory Affairs | Sr. Manager
Curium

Izabela Rejdych

EU Regulatory Affairs Manager, Advanced Accelerator Applications
MSc Pharmacy, MSc Pharmacology
More than 7 years of experience in global Regulatory Affairs, including multiple RA procedures and lifecycle management activities in several geographical locations (EU, US, Switzerland, ROW countries).

Eric Guilbert

Director, Commercial Operations Canada, Asia, Europe, Jubilant Draximage

Demet Kökoğlu

Senior Regulatory Affairs Specialist, S.C. Monrol Europe SRL
BSc. Chemistry, MSc. Pharmaceutical Technology / Pharmacy
More than 9 years of experience in Regulatory Affairs and more than 5 years of experience in Global Regulatory Affairs of radiopharmaceuticals including multiple regulatory procedures in several geographical locations (i.e. EU, Middle East ).

Helen Barker PhD, MTOPRA

Director of Regulatory Affairs
Blue Earth Diagnostics Ltd.

Philippe VanWolleghem

IRE

Joana Brilhante

Head of Clinical Development - ANMI

Tapashi Dasgupta

Manager, Global Regulatory Affairs - Nordion

Fatiha Siegwalt

Vincenzo Cannizzaro

RA -Global Regulatory Leader
Medical Services - GE Healthcare