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Arazy Group Consultants Inc.
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Suite of Products

LICENSALE 2.0 – Registration Management Platform

From an early start-up to an established multinational medtech company, Arazy Group regulatory technology and registration management platform is designed to suit your company’s needs, no matter its size, regulatory experience, resources, or goals.

Start by Finding the Right Solution for you

This sounds like you:

  • Your company is a manufacturer of medical or IVD devices or a regulatory consultancy
  • You need expert regulatory consultation for the new markets your company or your clients want to enter
  • You are looking for a one-stop solution to get your or your client’s product(s) to market as efficiently as possible

This sounds like you:

  • Your company is a manufacturer of medical or IVD devices
  • You already have regulatory expertise for the new markets your company wants to enter
  • You are looking for an advanced and affordable registration software to easily manage your regulatory processes in-house

Your Regulatory Solution

Blue and grey circles used in Licensale logo

LICENSALE®

global medtech registration system

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Your Regulatory Solution

REGISLATE®

medtech registration management software

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Change Happens. We Get It.

Arazy Group gives your company the flexibility to switch from one product to the other as your regulatory needs change.

Want extra users to help manage projects? Easy.
Need expert regulatory advice for a new market? We’re on it.
Looking for an authorized representative to stay in compliance? Consider it done.

Get Started with a Product Tour →

Arazy Group Consultants Inc. is an international consultancy spanning several continents, assisting medical and IVD device companies with regulatory compliance and affairs as they try to enter new markets

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Regulatory Solutions

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Head Office

#200-1333 Johnston St., Granville Island,
Vancouver, BC V6H 3R9

PHONE: +1 604.681.6888
FAX: +1 604.681.6822
[email protected]

© Arazy Group Consultants Inc. - is an international consultancy spanning several continents, assisting medical and IVD device companies with regulatory compliance and affairs as they try to enter new markets
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