Arazy Group (1995) is the innovator behind the most effective and widely used MedTech regulatory technology products, LICENSALE®- Global Medtech Registration System and REGISLATE® - Global Medtech Registration Management Software (RMS). Used by thousands of regulatory affairs professionals since 2013, the company solutions facilitated over 4500 Medtech product registration activities in 140 countries worldwide. Unprecedented KPI in submission preparation time, fastest time to market, and state-of-the-art global registration information and management capabilities develop a community of "Regulatory Rockstars" driven to make advanced medical products available to practitioners and patients worldwide while allowing the MedTech industry to grow.
Our Regulatory Affairs experts at Arazy Group have designed the REGTalks series to share the most timely and relevant information with the MedTech Regulatory Industry. We believe these updates should be readily available & easy to access.
Regulatory information
Online/ in-person 60 to 90 minutes presentations focused on regulatory overview and updates for a specific country or group of countries and presented by regulatory affairs professionals and country experts, designed for Regulatory affairs professionals or international/ regional sales managers who want to enter the subject country or group of countries. It complements our bi-weekly, regularly updated short video series on YouTube.
Regulatory technology and information
Online recorded and live presentations focused on regulatory technology for managing marketing licenses and new product registration activities in a specific country or group of countries. Created for regulatory affairs professional or international/ regional sales manager who wants to enter the subject country or group of countries faster and more effectively through the use of regulatory technology solutions, systems, and software.
Jumpstart Workshop
Full two hours of hands-on training on how to use the Arazy Group LICENSALE system and REGISLATE software. Learn how to JUMPSTART Medtech product registration in 140 counties with a device-specific license application and country-specific registration process management in a matter of minutes. The workshop is designed for Regulatory affairs personnel who wish to transform their profession through regulatory technology solutions, systems, and software.
Share the knowledge
A semi-annual online event presents numerous medtech regulatory affairs professionals and industry service providers, discussing their experience implementing new processes and advanced solutions in their daily work. RegTalk Forum is a stage for anyone in the global regulatory affair community who wishes to take their practice to the next level.
