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Tools to support the design and assess the quality of active travel interventions and schemes.
Design, build and operate APIs in a consistent way
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
Results of past design and design right decisions issued by us since 2013.
The rules you must follow to make sure deer can be traced to help prevent and contain disease.
Part of a series collecting key facts and figures on new homes and regeneration.
Guides councils in preparing planning policies on housing for older and disabled people.
FCDO travel advice for Germany. Includes safety and security, insurance, entry requirements and legal differences.
How to assess household and non-household packaging from 2024 onwards if you’re a UK organisation affected by extended producer responsibility (EPR) for packaging.
Get help to classify herbal medicines, vitamins, food preparations, supplements and tonics for import and export.
One-day GDS Academy course on the importance of research and design in government.
How to unload, handle and hold animals at sites where animals not for human consumption are killed, and how the site must be designed.
This guide illustrates how well-designed places that are beautiful, enduring and successful can be achieved in practice.
How to use a before-and-after study to evaluate your digital health product.
When and how you need to register your item or apply for an exemption certificate to deal in ivory.
Records that must be kept when supplying or administering veterinary medicines in the UK.
How investigators and sponsors should manage clinical trials during COVID-19
How a product complies with EU safety, health and environmental requirements, and how to place a CE marking on your product.
Understand how to use artificial intelligence ethically and safely
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