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June 2, 2021
Up to this point, Switzerland have been able to be part of the EU for the Medical Devices industry. However, from the Date of Application of the EU Medical Devices Regulation (MDR) on May 26, 2021, Switzerland will become a “third country” as regards medical devices. Switzerland has the same regulatory status as UK for medical devices.
May 6, 2021
The Massachusetts Medical Device Development Center (M2D2) is a lifeline for the state’s smaller medical device companies, offering inventors and executives easy, affordable, and coordinated access to world-class researchers and resources at the UMass Lowell and the UMass Medical School campuses of the University of Massachusetts. See our M2D2 Sponsors.
April 5, 2021
The UK Medicines and Healthcare products Regulatory Agency (MHRA) has published new guidance on registration requirements and deadlines for medical devices and IVDs effective January 1, 2021 for some products.
February 22, 2021
Why RQMIS is your Best Option? No hidden fees! Our procedures comply with EU REGULATION (EU) 2017/745 for AR companies. Our prices are competitive with other ARs, BUT our basic price structure includes ALL of the required responsibilities of an AR.
July 23, 2020
The future of healthcare is going digital. Are you coming along for the ride?