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Register to vote Register by 18 June to vote in the General Election on 4 July.
Get endorsement for the Global Talent visa to work in the UK as a digital technology expert - fintech, gaming, cyber security, artificial intelligence
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
DCMS is launching the Media Literacy Taskforce Fund to award grant funding to projects piloting new methods of delivering media literacy interventions to ‘hard to reach’ citizens.
Below outlines the CAC’s jurisdiction for The Transnational Information and Consultation of Employees Regulations.
Guidance on the planning for mineral extraction in plan making and the application process.
Helping public health practitioners conducting evaluations – identifying when it is possible and appropriate to evaluate.
Design, build and operate APIs in a consistent way
Reduce development overhead and time to deployment by standardising how teams design, launch and manage APIs in your organisation.
How to use an ethnographic study to evaluate your digital health product.
How to show MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
Find out about the different simplified declarations for imports and what you need to do to get authorisation to use them.
This page provides practical information to help you make the most of your IP when doing business in India.
Information for healthcare professionals on how pulse oximeters are regulated, home use and issues to look out for when using the devices
Why it's important to evaluate digital health products that have been developed rapidly and how to choose evaluation methods in these circumstances.
Details of the process changes for established medicines, effective from 1 March 2024, which apply specifically to chemical products.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
Information to help you identify if your organisation needs to publish a modern slavery statement.
When a material is waste, is a by-product or meets ‘end of waste’ status.
How to import animals and animal products to Great Britain (England, Scotland and Wales), the Channel Islands and the Isle of Man from non-EU countries.
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