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How to get a parallel import licence for your medicine in the UK, including pharmacovigilance requirements and submitting your application.
Actions that parallel exporters to the EEA and intellectual property rights holders need to take.
The process to convert Parallel Distribution Notices (PDNs) into Parallel Import Licences (PILs)
Use the case studies to help you decide when your goods may (or may not) go beyond insufficient production.
Use these general provisions to help you determine the origin of your products.
Find out how the VAT Capital Goods Scheme (CGS) works, the items covered by the scheme, the rules and how adjustments and disposals are affected.
Check what processes are considered as insufficient production under the Trade and Cooperation Agreement.
How to assess household and non-household packaging from 2024 onwards if you’re a UK organisation affected by extended producer responsibility (EPR) for packaging.
How to use a crossover randomised controlled trial to evaluate your digital health product.
Parallel import licences granted in 2024
How UK organisations that supply or import packaging should comply with extended producer responsibility (EPR) for packaging.
How to get plant breeders' rights and what protection it gives your plant varieties.
Guide to licensing procedure and other restrictions for export of controlled dual-use items, software and technology, goods for torture and radioactive sources.
A guide to collecting data about your packaging. This is for UK organisations affected by extended producer responsibility (EPR) for packaging.
Don’t include personal or financial information like your National Insurance number or credit card details.
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