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Data, Freedom of Information releases and corporate reports
How to use an interrupted time series to evaluate your digital health product.
Consistent and standards-based comma-separated values (CSV) files help make data more effective and easier to share across government.
Details of sediment and sample analysis for marine licence applications.
Find out about how we manage unacceptable behaviour consistently and fairly.
How to show MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
Find out how to get support if you or someone you know is a victim of antisocial behaviour.
How to use an ethnographic study to evaluate your digital health product.
This toolkit is for Innovation Passport holders following the Innovative Licensing and Access Pathway (ILAP) and provides activities to support the design and development of medicines.
The latest reproduction number (R) and growth rate of coronavirus (COVID-19).
Guidance to government departments on the RPC's scrutiny process.
The Committee is running a landscape review of the institutions, processes and structures in place to support high standards of conduct.
A framework to help schools to collect information about their income and expenditure.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
How we assess issues of potential regulatory concern
This guide explains how impacts on local environment should be incorporated into a cost benefit analysis.
The UK government's design principles and examples of how they've been used.
Keep up to date with the latest information from the UK GLP monitoring authority.
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