Learn more about how our technical specialists can review and confirm your product’s readiness for market.
As a manufacturer of software as a medical device, you must ensure that you meet the relevant regulatory requirements before placing your product onto the market; for the EU, these are outlined in the Medical Device Regulation (MDR) (EU) 2017/745 and, for the UK, the UK Medical Devices Regulations (UK MDR) 2002.
Find out how our technical specialists can support your medical device software business
We provide a wide range of free webinars to help support your business
We offer a comprehensive range of medical device training courses
Read our whitepapers and articles to learn the latest on the medical device industry