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Mission Statement Group Activities


Regulatory Affairs: Group

Gunhild Paulsen, Chair

 


 

Regulatory Affairs Project Manager
PETNET Solutions (Siemens Healthcare Sector)
Degree in Law from University of Oxford, England

 

 

Robert Cantineau


Pharmacist since July 1974 from University of Liège (Belgium)
Doctor in Pharmaceutical Sciences and Radiopharmacist since 1982
Dire
ctor Regulatory Compliance Best Medical since 1991

Jean-Marc Decomps


Director General Cyclopharma Laboratoires

Didier Garonnat

 

Responsible Pharmacist & Quality  Assurance/Regulatory Affairs, IBA Molecular

 

 

 

 

 

Cecile Dumas,PhD.


PhD in Organic and Bioorganic Chemistry from the University of Pierre et Marie Curie in Paris;
Junior scientist at PSI (Paul Scherrer Institute, CH) and Menarini Ricerche (I);
Quality Assurance Manager, University Hospital Zurich (CH)Regulatory Affairs Consultant, Nipcos (CH)
Quality and RA Manager, SWAN Isotopen AG (CH)

Claire Hill-Venning

 

Regulatory Oncology Group Head,
GE Healthcare

 

Hester Larkin


Lantheus Medical Imaging
MD of Hester Larkin Associates Consultancy
25 yrs experience in the Pharmaceutical Industry.

Last 12 years as European Managing Director for Dupont Pharmaceuticals and latterly BMS Medical Imaging

Pierre-Marie Lemer


President & Director General LEMERPAX

 

Michael Nader

Study of Chemistry (University of Heidelberg);
PhD in Radiopharmaceutical Chemistry (German Cancer Research Centre, Heidelberg);
Research Associate, Duke University Medical Centre, Durham, NC (USA).
Production Manager International, Head of R&D at IASON GmbH.

 

Mika Nyyssönen
 

Managing Director
MAP Medical Technologies

 

 

 

Agelos Pagonis
 


30 years experience in the nuclear medicine field.
President and CEO, Biokosmos
.

 

Laetitia Schlachter
 

Pharmacist/Master's Degree in Health Law
Regulatory Affairs Manager at Advanced Accelerator Applications (AAA)

 

 

Ibis Sundus
 

Regulatory Affairs & Pharmacovigilance Manager
Monrol Europe

 

 

 

 

Julien Thonnart
 

Industrial Pharmacist
Regulatory Affairs Manager, IRE - Institut des Radio Elements

 

 

 

Gerhard Vollberg

1987 Degree in Pharmacy, University of Bonn, Germany
1992 Ph.D. degree in medicinal/analytical chemistry, University of Bonn, Germany
17 years experience in European regulatory affairs

Director Regulatory Affairs EMEA Covidien Pharmaceuticals