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Reports, analysis and official statistics
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Data, Freedom of Information releases and corporate reports
The Committee is running a landscape review of the institutions, processes and structures in place to support high standards of conduct.
Your purchasing strategy must show you’ve considered commercial and technology aspects, and contractual limitations.
When you have to take a motorcycle trainer standards check, what happens at the check and how your result is worked out
What is involved in regulatory judgements and gradings
Guidance for hospitals, tissue establishments and fertility clinics for ensuring the quality and safety of human organs, tissues and cells (including reproductive cells).
For manufacturers of long-term samplers and test laboratories who carry out testing of equipment.
Our regulatory standards set the outcomes that social landlords in England must deliver for tenants.
Formerly part of M18, how to prepare and interpret analytical quality control (AQC) charts to verify the performance of your monitoring method.
Advice for medical professionals to follow when assessing drivers with visual disorders.
How to choose data tools and infrastructure that are flexible, scalable, sustainable and secure.
Standards, requirements and guidance for social landlords in England on transparency, influence and accountability, including Tenant Satisfaction Measures (TSMs).
Find out what you must include in an air dispersion modelling report to get an environmental permit.
The report sets out the Regulator of Social Housing's annual review of its consumer regulation work in 2023/24 and includes case studies and lessons learned.
You can become a DVSA enhanced rider scheme trainer if you want to train fully qualified motorcyclists in the scheme
How the ESFA will apply minimum standards for 2018 to 2019
The standards set out what it takes to be a safe and responsible driver, rider or cyclist, and to provide training to drivers, riders and cyclists.
This is collated guidance from government websites and independent bodies to help you follow the technology code of practice.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
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