Ensuring compliance throughout deployment

Medical device standards and regulations define surveillance and monitoring processes that must be undertaken by the product owner, or manufacturer. Failure to comply with these requirements carries stringent penalties.

The image shows a female administrator sitting in a hospital at a desk with a telephone looking at the two screens in front of her. One screen shows a list of patients, the other shows a list of surgical procedures.
In collaboration with C2-Ai we have implemented sophisticated risk prediction algorithms into routines that assist hospital teams to prioritise patient waiting lists to ensure patient safety. This system is in routine use in multiple NHS hospitals and trusts. We are responsible for all aspects of its deployment. We full comply with the requirements of the NHS.
Camgenium has the capabilities and experience to take responsibility for your legal requirements throughout deployment.

Jane Aldridge

CFO

Your alternative is to recruit a specialist team and purchase the necessary capabilities to manage your product deployment. Rather than take on the management burden and risk, it makes sense simply to transfer this function to Camgenium.

Product decommissioning is also complex and must be undertaken to standards. We have extensive experience of all these aspects of medical device lifecycle management and can ensure that your regulatory and legal tasks are executed correctly and to full standards.

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