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GlobalMed Announces Compliance with European Medical Device Regulation (MDR)

GlobalMed

Suite of CE marked software and devices meet the new, stricter medical device standard. . MDR is a new set of regulations that governs the production and distribution of medical devices in the European Union and will be mandatory for companies that want to sell these products in that marketplace.

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GlobalMed Celebrates 20 Years Offering Virtual Health Technologies

GlobalMed

In celebration of its 20th year, GlobalMed announces its newest initiatives for expanded access to care and support of federal, commercial, and international customers. When GlobalMed’s CEO and Founder, Joel E. 2021 was a banner year as GlobalMed adds to its security profile. SCOTTSDALE, Ariz. New product launches.