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Guidance on choosing evaluation study types and methods.
Compare different evaluation approaches and choose an appropriate method.
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.
Technical advice and guidance for licence holders.
How to use usability testing to evaluate your digital health product.
Get endorsement for the Global Talent visa to work in the UK as a researcher or academic leader - fellowship, UKRI endorsement, peer review.
Following MHRA approval of a clinical trial, a study on Nuwiq, a recombinant FVIII therapy for the treatment of haemophilia A, can proceed.
This guidance explains what rules of origin (RoOs) are and the changes under the Developing Countries Trading Scheme (DCTS).
How to use a micro-randomised trial to evaluate your digital health product.
Helping public health practitioners conducting evaluations – choosing evaluation methods.
Planning the practicalities and managing or conducting your evaluation.
How to use focus groups to evaluate your digital health product.
Guidance on how to license electronic cigarettes and other inhaled nicotine-containing products (NCPs) as medicines in the UK.
Actions that trial sponsors should consider to build resilience into clinical trial design
How to use a clinical audit to evaluate your digital health product.
Information on trade sanctions, arms embargoes and trade restrictions, including trade controls, transit controls and restrictions on terrorist organisations.
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