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.

Read more: Gideon Elkayam

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.

Read more: Doram Elkayam

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.

Read more: Sandra Ferretti

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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Mr. Webster managed MDCI Ltd’s medical device consulting and European Authorised Representative business in the UK from 1997 until 2010.  He has over 40 years of quality assurance, regulatory and management experience.

Read more: John L. Webster

For manufacturers located in the United States with an interest in introducing their products (Medical Devices, In-Vitro Diagnostics, Cosmetics & Others) onto the European Market, the USA Branch Manager is responsible for all contact and service. 

Read more: Stacy Edelen

For manufacturers located in Israel with an interest in introducing their products (Medical Devices, In-Vitro Diagnostics, Cosmetics & Others) onto the European Market, the Israeli Branch Manager is responsible for all contact and service. 

Read more: Hemi Zimmerman