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DASA seeks innovations to enhance operational advantage through improved self suffiency and energy innovation
How to volunteer as a magistrate, who can and cannot apply, the application form, and what magistrates do in court.
Magistrates are volunteers who hear cases in courts in their community.…
To be a magistrate you must meet some eligibility requirements.…
Before you can apply, you must: visit your local court or research how…
300,000 early birds file their Self Assessment tax return in the first week of the new tax year.
Find out how well your organisation complies with the principles of the surveillance camera code of practice.
Advice on how to stay secure online from the UK's National Cyber Security Centre.
The review of the safety of isotretinoin has concluded.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
Claiming Universal Credit if you're self-employed - eligibility, reporting your earnings, start up periods
FCDO travel advice for St Kitts and Nevis. Includes safety and security, insurance, entry requirements and legal differences.
As part of the development of the Equality Measurement Framework, we commissioned research on “Measuring Inequality: Autonomy - The degree of…
Using an ecological momentary assessment to evaluate your digital health product.
Defence Secretary Grant Shapps provided an oral statement to the House of Commons on 07 May 2024, to update the House on a data incident involving activity by a malign actor.
This self-assessment checklist helps academy trusts check they are managing resources effectively and identify any adjustments they need to make.
Find out what the Self Assessment for Agents online service is for, what you can do in the service and how to do it.
Advice and guidance on the health needs of migrant patients for healthcare practitioners.
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 to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
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