Arazy Group Blogs and Case Studies 

Regulatory Update #190801– MDR 2017/745

Regulatory Update- MDR 2017/745 August 2019 The EU Commission recently released Additional Guidance Regarding the Vigilance System as outlined in MEDDEV 2.12-1 rev. 8.  This document provides additional guidance in relation to the Medical Device Vigilance System that...

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Regulatory Update #190701- MDR 2017/745

Regulatory Update- MDR 2017/745 July 2019 The new EU medical device regulations (MDR 2017/745) are almost here. They will be going into effect on May 2020 and will affect all medical devices. The focus of this document is the class I self-declared devices, which are...

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FDA Series- AMRA Medical

AMRA is a ground-breaking, international digital health company at the forefront of medical imaging and precision medicine. The company has developed a new global standard in body composition assessment, delivering multiple fat and muscle biomarkers with unrivaled...

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FDA Series- ETGAR Medical Instruments

Late last year, the Dental Implants: Global Markets to 2023 report, was published detailing the industry’s expected high competition levels and a market to exceed US $6.5 Billion by 2024. With this industry quickly growing, Arazy Group Consultants is excited to work...

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International MedTech Events You Should Know About

There has been more international medtech events in the recent years making it quite the decision as to which to attend! The following conferences and forums are the top events that you and your collegaues should know about and attend for the remainder of...

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Top MedTech Events You Need to Attend in 2019

Canada’s MedTech Conference Date: April 3-4th, 2019 Location: Mississauga, ON This Canadian conference was designed to create a better understanding of the current initiatives in healthcare and how MedTech can contribute to these initiatives. There will be sessions...

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RDC 270/2019 Summary

Changes for Low Risk Devices in BrazilAs of May 2019, there will be a new registration notification pathway allowing medical device manufacturers to access the Brazilian market quicker. The recently published RDC 270/2019 establishes this new notification pathway...

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Calling all Consultants!

Are you a regulatory affairs consultant looking to expand your service offerings to your existing clients and increase your client base?  Arazy Group is opening Licensale for consultants in the medical and IVD device industry who wish to develop their practice....

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FDA Series- SyntheticMR

With the MRI Systems market to reach $7.9 billion by the year 2023 and the USA being the biggest market for MRI globally, it was essential that SyntheticMR received FDA clearance for their post-processing MRI software, SyMRI (versions 10 and 11). The SyMRI...

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Do You Know Your MARI%™ Score?

MARI%™ - Market Access Readiness Index Score (1-100%) Do you know exactly how ready your medical and IVD devices are to enter new markets based on their current documentation? The access to this information is available with the MARI%™ - Market Access...

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