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Detailed guidance, regulations and rules
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Data, Freedom of Information releases and corporate reports
Responsibilities of accountable persons for a building’s safety case.
Guidance on managing and using bed rails safely.
How to prepare for implementation and compliance of the Safety Features Regulation.
How to design, inspect, monitor and maintain impounding reservoir spillways so they are safe.
Health and safety issues and regulations for farm vehicles, machinery and equipment: risk assessments and good practice.
Advice on writing clear notices and maximising replies to your FSNs.
Information and guidance on a range of medical devices for users and patients.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
The guide, toolkit and further information for GB authorities with responsibility for consumer product safety.
Things to consider when buying and using products.
This guidance provides leaseholders with a plain English explanation of the implications of the leaseholder protections in the Building Safety Act 2022.
Understand how preventative design measures can reduce the risk of harms happening on your online platform.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
This page brings together information leaseholders and other residents should be aware of on fire safety, and remediation of historic building safety defects – including who is responsible for paying for remediation works.
Information for patients, public and health care professionals.
This information explains what the Cladding Safety Scheme (CSS) is, how to apply, and the additional help in place to support leaseholders and residents affected by unsafe external wall systems.
A guide to farming risks, potential problems with public safety and how to avoid accidents
An overview of the changes made to the Railways and Other Guided Transport Systems (Safety) Regulations 2006 (ROGS) that came into force on 1 January 2021.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
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