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Reports, analysis and official statistics
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Data, Freedom of Information releases and corporate reports
Tom Winsor conducted an independent review of police officer and staff remuneration and conditions, published March 2011.
This collection brings together all documents relating to public bodies.
The UK government's design principles and examples of how they've been used.
What animal by-products (ABPs) are, how to set up a site that uses them safely, the paperwork you need, and how to dispose of them.
This playbook explains how we use social media at GDS. In it, we share our best practice, what we've learned and what we're planning to do.
Guidance on the many ways for suppliers to work with the Defence Science and Technology Laboratory (Dstl), the science inside UK defence and security.
Guidance for sponsor departments, arm's length bodies, review teams and lead reviewers about the Public Bodies Review Programme.
Get help to classify various types of vehicles such as mobility scooters, dumpers and utility vehicles, all-terrain vehicles and e-bikes for import and export.
Find out about group and divisional VAT registration and the forms you should use to apply.
General information for medical professionals about the assessing fitness to drive guide.
Sets out the process for efficient and inclusive consultation of planning applications
Resources for local regulators.
Environmental regulations and guidance on offshore oil and gas exploration and production, offshore gas unloading and storage and offshore carbon dioxide storage activities
Guidance on the content of a Development Consent Order required for a Nationally Significant Infrastructure Project.
Find out which supplies of children’s clothing or footwear are zero-rated for VAT.
Rules for feeding, watering, prioritising, holding animals for slaughter, and the design and layout of a slaughterhouse.
Investors and businesses may be legally required to tell the government about certain sensitive acquisitions under the National Security and Investment Act.
How the MHRA makes decisions on when a product is a medical device (borderline products), and which risk class should apply to a medical device.
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