Congress Speakers

  • Adi Ickowicz, USA / Israel / Belgium I Congress Chairperson

    Adi Ickowicz, USA / Israel / Belgium I Congress Chairperson

    Adi Ickowicz BSc, ME is the co Founder and CEO of MedicSense Ltd., a Clinical and Regulatory Affairs consultancy firm that specializes in assisting companies to navigate through the international clinical and regulatory maze. 
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  • Susan Alpert, USA

    Susan Alpert, USA

    Susan Alpert, Ph.D., M.D.is currently the principle of SFA Consulting LLC, a one person firm focused on the strategies needed to place medical devices into the global market. Dr. Alpert joined Medtronic in July 2003 as Vice President of Regulatory Affairs and Compliance. 
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  • Stephan Buttron, Germany

    Stephan Buttron, Germany

    Dipl.-Ing. Biomedical Engineering
    Principal Medical Research Manager, Regulatory and Quality Services, NAMSA
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  • Sylvie Framery, France

    Sylvie Framery, France

    Dr. Sylvie Framery, Senior principal medical research scientist at NAMSA, has 16 years of work experience primarily focused on the pre-clinical evaluation of medical devices. In the French NAMSA Laboratory, she serves as Technical Specialist in support of Medical Research Managers and Project Development Advisors.

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  • Ittipan Kanluan, Germany

    Ittipan Kanluan, Germany

    Ittipan Kanluan, Dipl.-Ing., is a Regulatory Affairs Expert in the field of Active Medical Devices / Medical Software at CE plus GmbH, an international service provider for medical devices and in vitro diagnostics based in Germany.
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  • Lea Koelemeijer, Netherlands

    Lea Koelemeijer, Netherlands

    Lea Koelemeijer is partner at Crefact consultants, based in the Netherlands. 
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  • Nicola Revellin, France

    Nicola Revellin, France

    Senior Medical Research Scientist |NAMSA
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  • Andrea Saud Martinez, USA/Brazil

    Andrea Saud Martinez, USA/Brazil

    Andrea Saud Martinez, brings more than 23 years of international management and clinical research experience.  Currently she is acting as General Manager for Latin America at ATLANTIS CLINICAL, CRO providing clinical trial support in Latin America. 
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  • Maurizio Suppo, Belgium

    Maurizio Suppo, Belgium

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

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  • Robert van Boxtel, Netherlands

    Robert van Boxtel, Netherlands

    Robert van Boxtel graduated with a MSc title in the field of biomedical materials from the University of Twente in the Netherlands.  For eight years he worked in the medical device industry in the Netherlands and USA, in different roles within R&D and manufacturing.

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  • Harry van Vugt, Germany/Netherlands

    Harry van Vugt, Germany/Netherlands

    Mr. Harry van Vugt – Certification Manager, Regulatory Medical specialist and Project Manager - DEKRA Notified Body.

    Mr. Harry van Vugt has many years of experience (since 1990) in the field of regulatory affairs, quality and certification of medical products. 

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