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Consultations and strategy
Data, Freedom of Information releases and corporate reports
How investigators and sponsors should manage clinical trials during COVID-19
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
How to use routinely collected data to evaluate your digital health product.
The Civil Service Leadership Academy immersive learning series.
Using an ecological momentary assessment to evaluate your digital health product.
This guidance provides information on comparator products used in studies supporting abridged marketing authorisation applications
This guide sets out who has to apply for a permit, how to apply and explains the other rules covering travel to Antarctica.
How to use interviews to evaluate your digital health product.
Apply for an Academic Technology Approval Scheme (ATAS) certificate, to study certain subjects in the UK.
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
An outline of the delivery patterns that are outside of standard delivery.
Guidance on how to license electronic cigarettes and other inhaled nicotine-containing products (NCPs) as medicines in the UK.
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
How to write up and share your findings
Helping public health practitioners conducting evaluations – using outcome evaluations to find out if an intervention works.
How to use a feasibility study when planning the evaluation of your digital health product.
Your rights to request time off for training or study while in a job
The Lambert toolkit is for universities and companies that wish to undertake collaborative research projects with each other.
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