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How to use a clinical audit to evaluate your digital health product.
Collection of European Trade Mark and Design Network common practice notices.
We are allowing alternative courses of actions for manufacturing or laboratory equipment during the outbreak.
You're required to keep records for all traded goods you declare to HMRC for four years, for duty and tax purposes and for government statistics.
Find out when you can zero rate books and other forms of printed matter.
Standardisation explained.
How to use a cost utility analysis to evaluate your digital health product.
Guidance on how to license electronic cigarettes and other inhaled nicotine-containing products (NCPs) as medicines in the UK.
Quality and labelling rules for growing, packing, distributing, importing and selling fresh fruit and vegetables.
Actions that trial sponsors should consider to build resilience into clinical trial design
How to use a contextual inquiry when developing your digital health product.
What driving instructors should do to carry out realistic mock driving tests, including what needs to be in the test, assessing faults and recording the result.
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 about working in collaboration with other charities.
Information for schools about the standard setting process for key stage 2 national curriculum tests.
Information for schools and local authorities about scaled scores and the expected standard for the 2023 national curriculum tests.
Guidance on Animal Test Certificates (ATCs) required to carry out the field trial of a veterinary medicine in animals (clinical trial) in the UK.
How to package medicines for sale and what information you must provide to consumers and healthcare professionals.
Guidance to help organisations choose a monitoring approach for stack emissions to air that meets Environment Agency and MCERTS requirements (formerly part of M2).
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