Dear Medical Devices Group member,
 
As a leading international company in the MedTech space, we share your enthusiasm for developing and bringing new medical technology and improved medical practices to physicians and patients around the world.
 
There is a faster, better and much simpler way to bring your product(s) to market. Any market. A way to obtain and own your product premarket approval independently of your distributor and generate additional revenue from multiple market access simultaneously.
 
LICENSALE.COM® has been used by small-sized to large multinational MedTech companies for over three years now, and it has proved to reduce overall regulatory costs by as much as 50% and expedite time-to-market by 100%.
 
It is the only online regulatory platform that provides:
 
• The most up-to-date, device specific regulatory intelligence for 100+ countries
• A license application template for each type of device in each market
• Online application preparation services including documents review by qualified experts
• A document manager and archiving tools
• Project management and progress reports
• Final dossier preparation
• Submission to authorities
• Local authorized representative and independent license holder
• Post marketing, license maintenance and renewal activities
 
We feel responsible for bringing this information to you and urging you or someone on your behalf to have a closer look at this technology. We are confident that it would significantly contribute to the success of your company and your professional career. Schedule a demo today, and see for yourself why everyone is talking about LICENSALE.COM®.


Benny Arazy
President & CEO

 
latest news
  • Apr 24 2017
    70+ CLASS I DEVICES NOW EXEMPT FROM 510(K) REQUIREMENTS

    The US Food and Drug Administration (FDA) has identified a list of over 70 class I devices that are now exempt from premarket notification requirements....

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  • Apr 19 2017
    REGULATORY UPDATE: ETGAR MEDICAL INSTRUMENTS

    USA: Etgar Medical Instruments' Dental Implants System was approved for sale with LICENSALE.COM®. ...

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  • Apr 19 2017
    RUSSIAN REGULATORS ISSUE REQUIREMENTS FOR IVD & MEDICAL DEVICE TECHNICAL FILE SUBMISSIONS

    The Russian Ministry of Health has introduced a new regulation that clarifies the official requirements for in vitro diagnostic (IVD) & medical device technical file submissions. ...

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  • Apr 6 2017
    REMINDER: ARAZY GROUP CAN HELP REGISTER MEDICAL DEVICES IN BRAZIL IN JUST 7-9 MONTHS

    As a member of ABIMED (the Brazilian Association of Industry of High Technology Medical and Hospital Equipments, Products and Suppliers), Arazy Group can help medical device manufacturers register their products in Brazil within seven to nine months. ...

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  • Apr 4 2017
    ARAZY GROUP OFFERS QMS UPGRADE TO ISO 13485:2016 STANDARD

    In line with its commitment to making safe and effective IVD and medical devices available worldwide, regulatory affairs firm Arazy Group Consultants Inc. is assisting MedTech manufacturers in meeting the deadline to upgrade their quality management syste...

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VANCOUVER OFFICE

  • Phone +1 604.681.6888
  • Fax +1 604.681.6822
  • info@arazygroup.com
  •  
  • #350-1333 Johnston Street
  • Pier 32, Granville Island
  • Vancouver, British Columbia
  • Canada V6H 3R9

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