Medical Device Ce Marking Articles & Analysis
2 articles found
The Medical Device Directive 93/42/EEC (MDD) is a regulation that sets out the essential requirements that medical devices must meet before they can be placed on the market. ...
The global COVID-19 pandemic has spurred on a new demand for diagnostic equipment and products in the race to minimise spread. Airports, workplaces, border checkpoints, hospitals and countless other facilities - they’ve all needed accurate qPCR testing capabilities. ...