News
The latest news from NHS Kent and Medway.
For media enquiries, contact kmicb.engagecomms@nhs.net.
Subscribe to our newsletter.
A new social licence has launched to guide how health and care organisations in Kent and Medway use and protect public data.
"Our Data, For Our Good: How we use your information to help us all" , a lso known as the Kent and Medway Social Licence, has been co-designed by the NHS Kent and Medway Digital and Data Involvement Group and digital and data leaders, to make sure the views of people and communities fe e d directly into the development of projects on data.
The five principles have been adopted by the Kent and Medway Integrated Care System (ICS) and set the standard for responsible and transparent use of health data in Kent and Medway.
Image: Digital and Data Involvement Group members.
The Kent and Medway Digital and Data Involvement Group was set up in April 2025 , bringing together local and diverse voices to support the co-design and co-production of the social licen c e.
Two in-person workshops were held in May and June 2025, followed by additional virtual workshops throughout the year.
Over 50 people were involved, including digital and data leads from health and care organisations, Kent County Council, Social Enterprise Kent, Healthwatch Medway, Healthwatch Kent, Rethink MIND, Nigerian Association and Youth Ngage Kent .
Mayur Vibhuti, chief clinical information officer, NHS Kent and Medway, said: “Data has become one of the most valuable tools we have in improving peoples' health and wellbeing. It helps us see patterns, plan services, and understand what works, but it's also deeply personal. That's why trust and transparency must sit at the heart of how we use it.
“ Our communities want to know how their information is being used and how it can benefit them. The Kent and Medway Social Licence is our commitment to being open, honest, and accountable empowering people to have choice, confidence, and control. ”
Michelle Gardener , chair of the digital and data involvement group, said: “It i s significant that our communities have co-designed the principles. A social licence lays the foundation for trust and confidence in how data is handled and used.
“That means these principles must go beyond light-touch definitions on a page and directly shape how the system acts in practice; ensuring people are actively informed, respected and given clear information around their rights and choices.”
“ We recognise the commitment of our digital and data involvement group, our digital citizens - whose energy and insights have ensured that the voices of our communities of Kent and Medway entered the room with us and have been both, amplified and reflected in this work."
Isabel Clark, s trategic community partnerships and insight lead for Health Innovation Kent, Surrey and Sussex , said: “Working with people and communities through a co-production approach with the Digital and Data Involvement Group has greatly enhanced the use of data in Kent and Medway .
“The launch of Our Data, for Our Good marks the beginning of a long-term effort to build public trust in the use of health and care data, focusing on trust, consent, and confidence.
“As the use of NHS health data continues to grow, we will continue to ensure community voices are central to how data is used in Kent and Medway .”
Read the Social Licence methodology: From Data to Trust Community Voices in Kent Medway and Sussex Social Licence Methodology.docx [docx] 196KB.
Principle 1: Listening to communities
We will make sure local people are at the heart of making decisions on use of data .
We will speak with local people regularly about this.
We want local people to feel respected and involved in data use.
Principle 2: Honest and clear
We will be as honest and clear as possible about how data is used.
We will tell you what you need to know on who is using data, why, and how.
We will tell you how data use helps you and local residents .
We only use data for specific reasons and will tell you if this changes .
Principle 3: Keeping data safe
We will use the most up to date and robust security measures to protect people's data. We will explain what we do to protect people's data. If something goes wrong, we will explain what happened and how we will fix it.
We expect all organisations such as non-NHS organisations to follow the same high standards . People (not just computers) will always check how data is used, this includes the use of Artificial Intelligence (AI).
Principle 4: Your choice
We will tell you about your rights and choices when it comes to using your data.
We will explain what happens if you choose to say no (opt out) to data use, and we will do this in a fair and honest way - without trying to pressure you .
We respect that people want more control over how their health data is used.
Principle 5: Fair and correct data
We agree to use data in a fair and equal way, listening to concerns people may have around data use, this includes people who have poorer health outcomes .
We will tell you about your rights, the risks, and the benefits of data use.
We will work hard to keep data correct and up to date. We will also urge people to check their own records to make sure their data is right.
Everyone - along with staff and the public - shares the job of making sure data is correct.