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Learn how to check if your website or mobile app is accessible.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
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.
Guidance on Defence and Security Accelerator terms and conditions for funding, contracts and intellectual property rights.
Find the notes for all Declaration Category Data Set tables covered by Appendix 21-25 of the CDS Declaration and Customs Clearance Request Instructions.
This guide provides an overview of the regularly produced economic statistics and the relevant international standards for them
How to show the MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
How a product complies with EU safety, health and environmental requirements, and how to place a CE marking on your product.
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