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Recognised bodies, listed bodies, recognised universities, accredited higher learning institutions, bogus degrees
You can check if a degree you’re studying for is officially recognised. If…
Recognised bodies are higher learning institutions that can award degrees.…
Certain bodies or institutions can award their own unique degrees. These…
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
Get endorsement for the Global Talent visa to work in the UK as a researcher or academic leader - fellowship, UKRI endorsement, peer review.
With a Global Talent visa you can work in the UK in academia or research,…
You can get fast track endorsement for the Global Talent visa if you have…
You can get fast track endorsement if you have held an eligible fellowship…
You may be eligible for endorsement if you’re working on a research grant…
If you’re not eligible for another route, you may be able to get…
You can ask for a review if you do not think your endorsement application…
This collection page brings together investigation reports published by the Independent Inquiry into Child Sexual Abuse.
The Competition and Markets Authority (CMA) investigated the Atlantic Joint Business Agreement between American Airlines, members of International Consolidated Airlines Group (British Airways, Iberia and Aer Lingus) and Finnair under Chapter I of the CA98.
Student visa - check which courses you can study, prepare supporting documents, apply, what happens at the UK border
How manufacturers should undertake a clinical investigation for a medical device to ensure they comply with medical device regulations.
A series of reviews by Ofsted looking at the research evidence currently available about different curriculum subjects.
Find out about Corporation Tax relief you can claim for costs on R&D if you’re a small and medium-sized enterprise with an accounting period that starts before 1 April 2024.
How manufacturers in Northern Ireland should undertake a clinical investigation for medical devices to ensure they comply with EU medical device regulations.
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