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Transport analysis guidance (TAG) provides information on the role of transport modelling and appraisal.
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.
How investigators and sponsors should manage clinical trials during COVID-19
A National Travel Survey factsheet based on a view of mode use into a travel week from 2005 to 2015.
How to use an ethnographic study to evaluate your digital health product.
Use this tool to find out if you need to apply for a simple bespoke or complex bespoke medium combustion plant permit.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
Complete Self-Assessment form F3 or F3(S) for proposed, new and upgraded CHP Schemes
This guidance specifies the standards for the continuous monitoring and sampling of stack emissions.
How to use a crossover randomised controlled trial to evaluate your digital health product.
The rules on working hours - hour and limits, rests, health assessments and terms and conditions
This guide provides an overview of the inspection data summary report (IDSR) for primary and secondary schools, including schools with a sixth form and gives guidance on interpreting the data.
A guide to the major publications related to excess deaths in the UK, who produces them and links to the methods and analysis.
How to carry out a risk assessment if you are applying for a bespoke permit that includes discharging hazardous chemicals and elements to surface water.
Formerly part of M18, technical guidance for industrial plant operators (and their contractors) who monitor effluent discharges to water and sewer.
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