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How to use a combination of quantitative and qualitative data to evaluate your digital health product.
Find out when you can zero rate VAT for advertisements and goods used for the collection of donations.
How to use an N-of-1 study to evaluate your digital health product.
Apply to manufacture Extemporaneous preparations, Autogenous vaccines, authorisations for Equine Stem Cell Centre (ESCCA) or Non-Food Animal Blood Bank (NFABBA).
Customer declaration of specific uses of the scheduled category 1 or 2 substances (individual transactions).
Apply for a Temporary Work – Government Authorised Exchange (GAE) visa for work experience, training, research or fellowship - eligibility, extend or switch, family members
Export controls on goods that can be used for torture or capital punishment.
How a product complies with EU safety, health and environmental requirements, and how to place a CE marking on your product.
Guidance to help organisations choose a monitoring approach for stack emissions to air that meets Environment Agency and MCERTS requirements (formerly part of M2).
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
How to use a single commodity code to import your goods in split consignments when importing large machinery or plant.
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.
Submissions related to human medicines need to be submitted directly to the MHRA.
This Procurement Policy Note (PPN) updates the Selection Questionnaire (SQ) and accompanying statutory guidance and replaces PPN 03/23.
Find out if your university qualification means you're eligible for a High Potential Individual visa.
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
Guidance for manufacturers, importers and distributors.
An overview of the future requirements for rapid COVID-19 diagnostic assays for antigen lateral flow devices.
How to get relief from excise duty on oil used in certain ways using the Industrial Relief Scheme, also known as the Tied Oils Scheme.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
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