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Detailed guidance, regulations and rules
Reports, analysis and official statistics
Consultations and strategy
Data, Freedom of Information releases and corporate reports
Find out about local procedures, burials and cremations, and returning the body to the UK.
Find out about applying for the Spirit Drinks Verification Scheme, how to submit brand information, fees and making sure your production process is compliant.
Helping public health practitioners conducting evaluations on how to plan them.
How to evaluate digital outcomes, digital specialists and user research participants suppliers.
Information about when you need to submit substantial amendments to a clinical trial including changes to the trial sponsor or legal representative, Investigational medicinal product certification and importation.
How to apply for the different simplified declarations for exports and what you need for authorisation to use them.
How to use a combination of quantitative and qualitative data to evaluate your digital health product.
Cyber Defence and Risk (CyDR) defence industry ICT accreditation and risk balance case (RBC) processes.
Follow this guidance with help from your CDDO adviser to categorise digital and technology activity in your pipeline.
The Local Plan examination process and the role the Planning Inspectorate plays.
Assessment methods you can use to find the right Digital Outcomes and Specialists supplier for your needs
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
The Technology Code of Practice is a set of criteria to help government design, build and buy technology.
Your purchasing strategy must show you’ve considered commercial and technology aspects, and contractual limitations.
Guidance for manufacturers, importers and distributors.
How to apply for marketing authorisation via this new procedure.
Emerging techniques on how to prevent or minimise the environmental impacts of industrial hydrogen production from methane or refinery fuel gas with carbon capture for storage.
The process for applicants applying for a Paediatric Investigation Plan (PIP) modification or waiver.
Guidance to help you plan and prepare for implementing artificial intelligence (AI).
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