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This collection contains immigration staff guidance about applications to study in the UK
An outline of the delivery patterns that are outside of standard delivery.
Guidance and tips for British nationals studying at university in the USA
Actions that trial sponsors should consider to build resilience into clinical trial design
How to use a randomised controlled trial to evaluate your digital health product.
Guidance for schools on writing statutory end of year reports for parents.
Helping public health practitioners conducting evaluations – developing a logic model to represent how your intervention works.
An overview of 16 to 19 funding.
The UK Good Laboratory Practice Monitoring Authority (UK GLPMA) recognises that there are potential challenges COVID-19 will present to members of the GLP monitoring programme.
How to use feedback from marketplace reviews to evaluate your digital health product.
What you need to do if you're planning to start higher education in the EU.
Emerging techniques on how to prevent or minimise the environmental impacts of post-combustion carbon dioxide capture.
Advice and guidance for students on how to cope with pressure associated with test and exam anxiety.
How to use a cost benefit analysis to evaluate your digital health product.
Student visa - check which courses you can study, prepare supporting documents, apply, what happens at the UK border
How to use a crossover randomised controlled trial to evaluate your digital health product.
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
Watch our caseworkers' top tips to make sure your applications are complete and correct. Avoid more than 20 common requisition points.
How to use interviews to evaluate your digital health product.
Using an ecological momentary assessment to evaluate your digital health product.
Don’t include personal or financial information like your National Insurance number or credit card details.
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