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How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
How to claim a VAT refund in the UK if you're established outside the UK.
Learn how to check if your website or mobile app is accessible.
How to ensure the products you make or import comply with the law and are safe for consumers to use.
How to make sure that your products are properly checked for conformity and your technical documents are managed correctly.
Guidance for local government and employers who need data on ethnic minority employment to set targets and monitor improvement in local areas.
The UK government's design principles and examples of how they've been used.
Information about which code you should open and how to do it securely.
Exporters of groups of products of animal origin (POAO) to the EU and Northern Ireland can join the groupage export facilitation scheme (GEFS) to use 30-day support attestations.
Prove the origin of your goods if you’re trading with a country that has a trade agreement with the UK, or is covered by the Developing Countries Trading Scheme.
Pharmacovigilance system requirements
Order a certificate of free sale to export medical devices outside the UK.
Find out if you need an Academic Technology Approval Scheme (ATAS) certificate to study in the UK.
Information and guidance on a range of medical devices for users and patients.
How to show MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
This page provides a collection of online media literacy resources and events.
You must get permission to export certain drugs and medicines.
This playbook explains how we use social media at GDS. In it, we share our best practice, what we've learned and what we're planning to do.
This guidance contains sources of support available to sponsors.
Guidance for manufacturers, importers and distributors on the Product Security and Telecommunications Infrastructure Act 2022 and Regulations 2023.
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