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Register to vote Register by 18 June to vote in the General Election on 4 July.
Who can apply to the scheme, how the application process works, and the checks that authorities must complete.
Reduce development overhead and time to deployment by standardising how teams design, launch and manage APIs in your organisation.
This rapid literature review examines impact and lessons in middle-income countries and fragile and conflict affected environments
This project improved understanding of hydrobiosedimentary processes and the problems caused by their interaction in estuaries.
This sets out the assessment and decision-making process for selecting successful bids to the Community Ownership Fund and the internal decisions approved by the Senior Responsible Officer (SRO).
Find out what you can do with your goods when they are being processed or repaired using outward processing.
Proficiency testing (PT), also known as external quality assessment (EQA), allows the introduction of samples of known but undisclosed content into a laboratory’s routine testing procedure.
Regulators must use this process guidance note (PGN) to assess applications and write permits for di-isocyanate processes.
Search reports on business payment practices: when invoices are paid, payment terms and practices
How to use a contextual inquiry when developing your digital health product.
Guidance and best practice documents for commercial systems and processes.
How GBN’s technology selection process for Small Modular Reactors (SMRs) will work.
Processes and principles used by the UK National Screening Committee (UK NSC)
Guidance on the fast-track process for Nationally Significant Infrastructure Projects.
The 12-stage process on how a marine plan is made from selection to implementation and monitoring and how you can get involved.
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
Your technology should adapt to future demands and work with existing technologies, processes and infrastructure in your organisation.
Find out when the Aggregates Levy does not apply to the intended products of an exempt process.
Submissions related to human medicines need to be submitted directly to the MHRA.
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