Mr. Gideon Elkayam has acted as Obelis’ C.E.O since Obelis’ creation on September 27, 1988. Through Mr. Gideon Elkayam’s hard work, leadership, code of ethics and always present drive for excellence, Obelis has managed to achieve important mile stones through the years.

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For any administrative matter (Agreements, terms and conditions, Invoices, Payments, Database and overall client relations & services) Obelis’ C.O.O. is the address. Involve Mr. Doram Elkayam on all matters allowing Obelis to insure the best service possible provided to you.

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With over 10 years experience in quality assurance and EU regulations, the C.C.O. is responsible for overseeing and managing compliance issues within the organization and ensuring internal and client compliancy.

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Dr. Peter N.  Ruys, an expert consultant in International Medical Device regulations. Founder of the Notified Body KEMA Quality in The Netherlands(1992-2004) ,one of the leading members in the initial implementation of the European Directive for Medical Devices, holds degrees in physics and chemistry from the University of Utrecht.

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With 13 years of experience in European Authorized Representative services and EU Regulatory Affairs for medical devices, in-vitro medical devices and overall EU New Approach directives, Miguel Ohn has been advising non-EU and EU manufacturers regarding a number of different regulatory matters.

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