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Guidance for the veterinary pharmaceutical industry on the production of mock-ups for assessment.
How to get a parallel import licence for your medicine in the UK, including pharmacovigilance requirements and submitting your application.
Add metadata to data you are publishing so search engines can find the data you’ve published and display structured results for users.
Help your team understand why they need to meet the website and mobile app accessibility regulations.
Check what you need to do if you're sending, receiving and storing VAT invoices in an electronic format.
Check what UIDs you need for your tobacco products and the specifications they need to meet.
How to use a think aloud study to evaluate your digital health product.
Building evidence for the creation of an efficient and future-facing system that can be rolled out nationally.
Information for EU citizens and their families applying to the EU Settlement Scheme.
Ofqual's formal legal list of Regulatory Documents (documents containing additional rules and guidance for regulated qualifications).
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