This message was posted by a user wishing to remain anonymous
I am currently working on timelines with our manufacturing and marketing team. We are a UK based company wanting to sell our class III device to the NHS
We are hoping to get approval for our medical device over the next couple of months
I am unsure however on the process and timelines between our notified body approving the product and when we can place our product on the market.
Do we need to wait for a hard copy of the CE certificate? Does the notified body have to inform MHRA and we have to wait for approval from them before selling our product? IS there any other registration or approval process to be able to sell to the NHS?
Thank you for your time