Posts in category EU MDR

View our EU Medical Devices Regulatio...

View our EU Medical Devices Regulation (EU MDR) Educational Webinar

November 15, 2018 |Written by GreenSoft Technology, Inc. Now Available to View On-Demand: EU MDR Webinar On November 14, we hosted a webinar on the new EU Medical Devices Regulation (EU MDR). Hosted by Randy Flinders, this educational presentation covered: An overview of the EU Medical Devices Regulation (EU MDR) Your responsibilities and requirements as […]

Register Now for EU Medical Devices R...

Register Now for EU Medical Devices Regulation Webinar

October 02, 2018|Written by GreenSoft Technology, Inc. Get prepared for the new European Medical Devices Regulation (EU MDR) coming in 2020 On Wednesday, November 14 we’ll be hosting a webinar about one of the most popular compliance topics in the industry: the new medical devices regulation coming out of the European Union. Compliance with the […]

Get Ready for the New EU Medical Devi...

Get Ready for the New EU Medical Devices Regulation

August 20, 2018 |Written by GreenSoft Technology, Inc. Compliance with New EU Medical Devices Regulation (EU MDR) Becomes Mandatory in May 2020 A new European regulation for medical devices is coming into effect in 2020. In May 2017, the EU Commission published the Medical Devices Regulation (MDR). The regulation becomes mandatory for medical device producers […]

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