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

Sandra van Leeuwen

Sr. Manager Regulatory Affairs (Head Regulatory Affairs)
Curium

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

Françoise Bruyère

Head of Clinical Operations and Regulatory
ANMI s.a., a Telix company

Tapashi Dasgupta

Manager, Global Regulatory Affairs - Nordion

Fatiha Siegwalt

Vincenzo Cannizzaro

RA -Global Regulatory Leader
Medical Services - GE Healthcare

Camelia Cercel

Director Regulatory Affairs
Advanced Accelerator Applications