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How to register your chargepoints for OZEV chargepoint grant schemes as a manufacturer.
When and how you need to register your item or apply for an exemption certificate to deal in ivory.
An overview of the future requirements for rapid COVID-19 diagnostic assays for antigen lateral flow devices.
How and when to identify pigs (livestock and pets) with ear tags, ear tattoos or slap marks so they can be traced.
Helping public health practitioners conducting evaluations – choosing evaluation methods.
Assessment methods you can use to find the right Digital Outcomes and Specialists supplier for your needs
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
Register for Annual Tax on Enveloped Dwellings (ATED) service to submit your returns online.
Advice and guidance on the health needs of migrant patients for healthcare practitioners.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
How to prepare for implementation and compliance of the Safety Features Regulation.
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.
Guide for suppliers on a Crown Commercial Service (CCS) commercial agreement, who supply common goods and services to the public sector.
The New Variant Assessment Platform (NVAP) is an offer of UK capacity and expertise to detect and assess new variants of SARS-CoV-2 around the world.
How to use a budget impact analysis to evaluate your digital health product.
How to use Method 1 to work out the customs value of your imported goods if you're an importer or clearing agent.
Advice on writing clear notices and maximising replies to your FSNs.
This guidance is designed to help UKHSA customers and partners to navigate engaging and working with us and to signpost upcoming events and opportunities.
How to use a factorial randomised controlled trial to evaluate your digital health product.
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