Company Profile

WE EXPEDITE SUCCESS of SAFE MEDICAL DEVICES

The Arazy Group is a world leader in Global Regulation of medical device and IVD products. We provide product registration services in more than 60 countries. We implement regulatory affairs strategies using the most advanced products, which allow multiple submissions through one comprehensive, quick and cost effective process. GlobaR™ - One World Process.

Traditionally, multiple-country regulatory compliance is achieved through separate, single submission processes. The common practice is fragmented, inefficient, costly and time consuming.

GlobaR™ regulatory intelligence system generates unique Global Master Regulatory File for any medical device, called a GlobaR™ dossier. Once the file is prepared any following registration is quicker and more efficient. Multiple country regulatory submissions are prepared in parallel and registration processes are executed simultaneously. The GlobaR – One World Process ™ creates one universal dossier that shows your device is safe and effective to be registered with any food and drug agency around the world. http://www.youtube.com/arazygroup

Whether you are seeking to enter your device into one market or multiple markets, we have the solution.

GlobaR™- One World Process™ - is patent pending.