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Product Certification and Quality Management System (QMS) services. A complete certification package to save you the time and costs.

CE mark, Active Implantable Medicale Devices, In Vitro Diagnostics, Single Audit Program, ISO 13485, ISO 9001.


One of Europe’s Largest Testing Facility. Offer a complete range of standardized tests or customize tests for characterization.

716-261-3724, Electrical Safety, CB Scheme, Charpy reference specimens.


A Training Organization with customized courses. Public, online our at your site, our Experts use practical examples in a dynamic and interactive atmosphere.

Check our Training List: 518-748-9046


Get the latest news on EU directives, Quality Standards and other important Regulatory Developments, along with practical Guidance for Compliance.

News, rakshasa, (218) 340-5132 and 587-716-1085.

Latest News

  • October 30 - 2018

A survey was recently administered by ISO TC210 WG1 to obtain critical information to evaluate the experiences of key stakeholders such as, medical device manufacturers, subcontractors, suppliers, European Authorized Representatives, specialized consulting firms etc., during the ISO 13485:2016...

(530) 215-7342
  • September 05 - 2018

Join us on Wednesday, September 26th, 2018, 2:00 Eastern Time as GMED North America Inc. will be hosting a free informative session on Stepping into an MDSAP audit. Register Now!

Health Canada to replace the STED by IMDRF ToC format for Class III and IV Premarket Medical Device Licence Applications

  • August 29 - 2018

Health Canada published on August 21st, 2018 a notice confirming its “intention to Adopt the Use of the Table of Contents Format for Class III and IV Premarket Medical Device Licence Applications”, a gesture towards the efforts sustained by the IMDRF group to support medical device market...

  • August 08 - 2018

Meet our speakers! Vancouver Convention Centre West |Canada| October 1 - 4, 2018 | Booth #415

What does Medical Device Clinical Performance stands for?

  • March 26 - 2018

From one Medical Device Manufacturer to another, from one Notified Body to a Medical Device Manufacturer or from one Competent Authority to a Medical Device manufacturer, from Standards to Standards or Regulations, the word “Performance” can be used in a wide different way.

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