Our Clients

LICENSALE.COM® has processed thousands of regulatory submissions for medical and IVD manufacturers of all sizes, from large, multi-national corporations to small start-ups. See a small sample of our clients below.

  • 3Shape
  • Abbott Research Group
  • Adlens Ltd.
  • AmbalSoft InfoTech Pvt.
  • Ameco Medical Industries
  • Bard Limited
  • Ecleris SRL
  • Elekta Limited
  • Equashield Medical Ltd.
  • FujiFilm SonoSite
  • Global Instrumentation LLC
  • Innocoll Pharmaceuticals Ltd.
  • KARL STORZ GmbH
  • Laborie Medical Technologies
  • Lexel Medical SRL
  • Luminex Corporation
  • ZELTIQ Aesthetics Inc.
  • Mitsui
  • Nihon Kohden Diagnostics Pvt.
  • Optos
  • Physio-Control Inc.
  • Revital Vision
  • Ritter Implants GmbH
  • Savion Industries
  • Trig Medical Ltd.
  • Varian Medical Systems
  • VisionSense Ltd.
  • Jon Yard
    Director of QA & RA for the EU & AFLAME (former)
    Elekta Limited, UK
  • Anna Le Bars
    Senior Regulatory Affairs Manager
    Luminex Corporation, USA
  • Rudolf Holzhausen, PhD.
    Hanin Medical
    Saudi Arabia
  • Azi Ben-Yishai
    VP Finance & Operations
    Visionsense Ltd., USA
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latest news
  • Jun 27 2017
    2017 RAPS: DON’T MISS INVALUABLE INSIGHTS ON REGULATORY STRATEGIES FOR MARKET ACCESS

    MedTech regulatory affairs professionals managing the launch of products in new markets and maintaining market approval globally will benefit from the invaluable insights shared during the ‘Regulatory Strategies for Market Access’ session at this year’s R...

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  • Jun 13 2017
    FDA TO REQUIRE NEW VALIDATION DATA FOR LIST OF REUSABLE MEDICAL DEVICES

    The US Food and Drug Administration (FDA) has unveiled a list of reusable medical devices for which it will require validation data regarding cleaning, disinfection and sterilization as well as validated instructions for use in premarket notification subm...

    Read More
  • Jun 11 2017
    SOUTH AFRICA: NEW REGULATORY AUTHORITY OVERSEES MEDICAL DEVICES

    Medical devices in South Africa are now regulated by the newly established South African Health Products Regulatory Authority (SAHPRA), which has replaced the Medicines Control Council (MCC)....

    Read More
  • Jun 7 2017
    FDA EXTENDS UDI COMPLIANCE DEADLINES FOR LOW-RISK MEDICAL DEVICES

    The US Food and Drug Administration (FDA) has extended the compliance deadlines for the unique device identification (UDI) system requirements for certain class I and unclassified medical devices from September 24, 2018 to September 24, 2020....

    Read More
  • Jun 5 2017
    AUSTRALIA: CONSULTATION ON COMPARABLE OVERSEAS REGULATORS FOR MEDICAL DEVICES OPENS

    Australia’s Therapeutic Goods Administration (TGA) is seeking comments from the MedTech industry and regulators on the use of marketing approval by comparable overseas regulators for medical devices in overseas markets to support the inclusion of them in ...

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