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Departments, agencies and public bodies
News stories, speeches, letters and notices
Detailed guidance, regulations and rules
Reports, analysis and official statistics
Consultations and strategy
Data, Freedom of Information releases and corporate reports
Guidance to help you manage the security of your devices and help protect your privacy
Research detailing cyber security issues in internet-connected devices used by businesses and organisations.
The home page for DSIT’s work supporting the secure and sustainable deployment of connected places technology, also known as smart cities.
Service providers or government departments installing networking technologies in government shared buildings, known as hub buildings.
Resources to help local authorities secure their connected places ("smart cities") against cyber threats. This is the updated beta release.
Product security factsheet accompanying the Product Security and Telecommunications Infrastructure Bill, outlining the problems the Bill will address and how.
How government is supporting research, development and demonstration of connected and autonomous vehicles, such as driverless cars.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
Guidance for organisations when making decisions about the design and operation of enterprise IT services which handle OFFICIAL information.
A collection of important guidance on the security of connected places, also known as smart cities.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
Information about the EU Regulations and their implementation in Northern Ireland
Information and guidance on a range of medical devices for users and patients.
How to conform with the legal requirements for placing medical devices on the market.
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
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