About the Arazy Group
The Arazy Group expertise is regulatory affairs and quality assurance for the medical device industry.
Arazy Group offers medical device registration services in more than 53 countries and have gained market clearance for medical devices and IVDs in North and South America, most European countries, various Asian markets, MENA, Africa and Australia.
We implement advance global regulatory products that enable our client to overcome the traditional; multiple-country regulatory compliance that is currently achieved through multiple-submission processes.
For more than 16 years, our professional consultants have utilized validation, verification and regulation processes on a diverse portfolio of medical devices,and are responsible for thousands of successful registrations globally. Our customized solutions accommodate all stages of medical device's life cycle and our adaptable services fit any application and any size organization.
Whether you are seeking to enter your device into one or multiple markets, we have the solution.
Specialties
Global Medical Device Registration, Medical Device Safety compliance, Quality Management System, Universal Representation & Administration, Clinical & Medical Research
New hires at Arazy Group
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Senior Regulatory Affairs Consultant
Came from...
Atrium Medical Corporation - Maquet Getinge Group, Director Regulatory Affairs
