Showing 91 to 95 of 112
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?
July 22, 2020
Is your product a medical device? Which classification has? Take a look at the steps needed to make this determination, and what it means for your product moving forward.
June 17, 2020
A look into this new category of products and the ways manufacturers are marketing them