Product safety
Intended use, local checks and what to do when information is unavailable or wrong.
Read the safety approachTrust centre
Trust is built through evidence, good questions and clear responsibilities. Here is how to approach the assessment of Bedbord and TESS.
A transparent starting point
Requirements depend on the product, software release, intended use and deployment setting.
This website does not publish verified ISO certificates, NHS DSPT status, a completed DTAC assessment, product conformity declarations or a clinical safety case. Their availability and applicability must be confirmed for the product you are assessing. Nothing here claims NHS approval or universal compliance.
Clarify controller and processor roles, data flows, lawful basis, retention, hosting and any international transfers.
Deployment reviewAssess whether DCB0129 and DCB0160 apply. Request release-specific safety documentation, residual risks and local deployment responsibilities.
Evidence to confirmDiscuss access controls, encryption, device updates, vulnerability handling, backups and incident response. Verify the implemented controls.
Evidence to confirmAsk for the exact hardware model, intended-use statement, relevant conformity documents, cleaning guidance and electrical-safety information.
Evidence to confirmTest with representative users, realistic lighting and placement, and the interaction methods needed in your setting.
Local assessmentConfirm supported interfaces, update responsibility, downtime behaviour, data freshness and a safe fallback.
Deployment reviewIntended use, local checks and what to do when information is unavailable or wrong.
Read the safety approachWhat the enquiry forms do with your information, and how to exercise your rights.
Read the privacy noticeWebsite features, known limitations and how to request another format.
Read accessibility informationA conversation is a good start
Bring your clinical, digital and procurement colleagues into the conversation.