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What providers need to know about registering with Ofsted and running or closing a supported accommodation service.
Create a mobile experience that meets user needs without relying on native or hybrid apps.
Submissions related to human medicines need to be submitted directly to the MHRA.
Business expenses you can claim if you're self-employed
Guidance for app developers, assessors and commissioning bodies involved in creating digital applications (apps) for public health.
Submit HM Land Registry applications in the portal, reducing errors and requisitions.
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
How to create a model of how your digital health product works and choose measures for your evaluation.
Follow this guidance if you’re a civil servant or government contractor to use cloud tools safely.
Foreign, Commonwealth & Development Office (FCDO) advice for lesbian, gay, bisexual and transgender (LGBT+) people travelling abroad.
Sets out process and expectations on pre-application discussions.
HM Land Registry portal users can use the View Applications service to manage portal applications and correspondence in one place.
Information about the EU Regulations and their implementation in Northern Ireland
If you're having trouble accessing a public sector website or mobile app, find out how to request alternative formats or report the issue to get it fixed.
How to download and access the HMRC app on a mobile device to get information about your tax, National Insurance, tax credits and benefits.
Guidance for manufacturers, importers and distributors.
How to use a crossover randomised controlled trial to evaluate your digital health product.
Information on when software applications are considered to be a medical device and how they are regulated.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
This guidance identifies common issues with validation and assessment of clinical trial applications and how to avoid them.
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