Call For Globally “Streamlined, Harmonized And Flexible Approach” To Real World Evidence
How A Medtech Conference Found Itself Focused On Tigers And Safaris.
Digital data capture is rife now in the medtech sector. What needs to be done at an international level to control and optimize its use and that of real-world evidence based on this data? Do initiatives that came up at the International Medical Device Regulators Forum offer solutions to prevent potential global chaos?
You may also be interested in...
With so many regulatory developments happening concurrently in the EU at present, five forthcoming conferences promise delegates a timely update and vibrant discussions.
With so much discussion now on the need for fundamental change in the future regulation of medtech products in the EU, Medtech Insight reflects on lessons to be learnt.
The EU medtech industry is calling for an update to the decades-old rules on electronic IFU for devices. A glimpse at the listings in the European Commission’s recently released table of member state language requirements reflects how punitive the demand for hard-copy IFU can be.