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
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