Congress Faculty

  • Mika Reinikainen, Congress Chair, UK

    Mika Reinikainen, Congress Chair, UK

    Mika Reinikainen is a founder and Chairman of the European Association of Authorised Representatives (EAAR) 
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  • Gideon Elkayam, Congress Co-Chair, Belgium

    Gideon Elkayam, Congress Co-Chair, Belgium

    Mr. Gideon Elkayam is the founder, owner and C.E.O since Obelis' foundation on September 27, 1988.    
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  • Bassil Akra, Germany

    Bassil Akra, Germany

    Dr. Bassil Akra is the global director of the clinical centre of excellence at TÜV SÜD Product Service GmbH. Dr. Akra has long experience in research, development, quality management and regulatory approval of medical devices, combination devices and ATMP products.
  • Oliver Bisazza, Belgium

    Oliver Bisazza, Belgium

    Based in Brussels, Belgium, Oliver Bisazza is Director, Regulatory Policy, Europe Middle East and Africa at Medtronic.
  • Ronald Boumans, Netherlands

    Ronald Boumans, Netherlands

    Ronald’s work currently focusses on Clinical Evaluation Reports for high risk devices, but he also helps manufacturers with strategic decisions
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  • Sandra Ferretti, Belgium

    Sandra Ferretti, Belgium

    With a near to 20 years of employment at Obelis s.a. as Chief Compliance Officer, Sandra Ferretti  has a unique expertise in European regulatory affairs both in cosmetics and medical devices fields. Her specialties: Regulatory affairs, cosmetics, medical devices, responsible person, authorized representation, quality assurance, policy making, European associations representation, company law, social law, business administration, public subventions. 
  • Robert Ginsberg, Sweden

    Robert Ginsberg, Sweden

    25+ years in SW Development 
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  • Amanda Maxwell, UK

    Amanda Maxwell, UK

    Amanda Maxwell is Medtech Regulatory Affairs Editor at Medtech Insight.
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  • Ludger Möller, Germany

    Ludger Möller, Germany

    President of Medical Device Safety Service GmbH (MDSS) 
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  • Maurizio Suppo, Belgium

    Maurizio Suppo, Belgium

    Maurizio Suppo, trained as a molecular biologist, has 30 years of experience in Quality & Regulatory in international medical device and in-vitro diagnostic industry.

  • Sarah Sorrel, France

    Sarah Sorrel, France

    Sarah Sorrel has more than 30 years of experience of medical device regulation and clinical trials with an emphasis on emerging technologies.
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  • Erik Vollebregt, Netherlands

    Erik Vollebregt, Netherlands

    Erik Vollebregt partner at Axon Lawyers

    Erik specialises in EU and national legal and regulatory issues relating to medical devices. He is an expert in life sciences regulation at EU and Dutch level.
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