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Would you like to join our Speaker Faculty?

If you are interested in speaking at the Medical Device and IVD Regulations in Russia, CIS, CEE and Turkey conference or would like to discuss an idea for a conference theme please contact:

Alison Preston: Tel: +44(0)20 701 77132 Email: alison.preston@informa.com

Expert Speaker Panel

Sinisa Tomic, European Affairs Counsellor, Croatian Agency for Medicinal Products and Medical Devices, Croatia

Branislav Radivojevic, Professional Assessor, Medical Devices Department, Medicines and Medical Devices Agency of Serbia, Serbia

Alexander Schapovalov, MHS – Foreign Affairs, TÜV SÜD Product Service GmbH, Germany

Dmitry Zubarev, General Director, The Center of Certification and Declaring, LLC, Russia

Enrico Schuur, Director Regulatory Affairs International, Medtronic International Trading Sarl, Switzerland

Kristina Mumber, Head of Regulatory Affairs EMEA, Novartis Vaccines and Diagnostics, Switzerland

Anna Firstova, Regulatory & Quality Manager, Zimmer CIS, Russia

Claudia Pres, Regulatory Affairs Manager EMA, Becton Dickinson, Germany (tbc)

Pavel Henčl, General Manager CIS Region, Gambro, Germany

Maria Obreztchikova, Sr. Regulatory Affairs Specialist, St. Jude Medical, USA

Alexander Berezin, Country Manager Russia and CIS, Edwards Lifesciences, Russia

Olga Orekhova, Regulatory Affairs Director Russia and CIS, GE Healthcare, Russia

Ondina Grigorescu, Regulatory Affairs and Quality Assurance Manager EEMEA, C. R. Bard GmbH, Germany

Tom Ståhlberg, Director, Government Affairs, Regulatory and Clinical Affairs, PerkinElmer, Finland

Andrey Ivanov, Group STM LLC, Russia

Keith Summerhayes, Managing Director & Clinical Affairs Consultant, MDCRQ Solutions Ltd., UK

 


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Dates and Venues

09 Oct 2012 - 10 Oct 2012

Continental Zara Hotel, Budapest, Hungary

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