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Helping public health practitioners conducting evaluations – using process evaluations to explain how complex interventions work.
Use these general provisions to help you determine the origin of your products.
Find out how to validate your facility when you seek approval to open, including special requirements for continuous and blood processors.
This guidance covers ‘grandfathering’ and managing the lifecycle changes of medicinal products.
We have more than 10 years’ experience of successfully working with our customers to develop solutions across the radioactive waste lifecycle and provide access to the full range of treatment, logistics, and disposal techniques and technology in the UK, Europe,...
Guide to licensing procedure and other restrictions for export of controlled dual-use items, software and technology, goods for torture and radioactive sources.
Find out the rules to establish the country of origin of imported and exported goods and to help identify goods which qualify for lower or no Customs Duty.
How to apply for accreditation, comply with your accreditation and packaging waste technical information.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
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.
Find out how you can use, process or store similar free circulation goods in place of goods that you have declared for a customs special procedure.
Find out if the goods you're declaring to inward or outward processing are classed as sensitive goods.
Using an ecological momentary assessment to evaluate your digital health product.
How to use a quasi-experimental study to evaluate your digital health product.
Find out what you can do with your goods when they are being processed or repaired using outward processing.
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
Information on how quickly we will process your application.
Check if you should submit a standardised exchange of information using the EU Customs Trader Portal for inward or outward processing.
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
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