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How you import from and export to the CARIFORUM States.
This guidance explains what rules of origin (RoOs) are and the changes under the Developing Countries Trading Scheme (DCTS).
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
How to begin with evaluating a digital health product, including when to evaluate, budgeting and getting support.
How to use usability testing to evaluate your digital health product.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
Assess your goods, software and technology to determine whether or not they are controlled and require a licence to export.
Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
Find out the information you must give to customers on food products and how to give it.
How the MHRA makes decisions on what is a medicinal product (borderline products).
How you import from and export to Mexico.
Search for information about medicines including patient information leaflets (PILs), details on how the medicine can be used (SmPCs) and scientific reports (PARs).
How you import from and export to Turkey.
Find out which regulations apply to your products and where to go for further information on how to comply with them.
Find a list of document status codes for Data Element 2/3 of the Customs Declaration Service (Appendix 5B).
Telecoms infrastructure factsheet accompanying the Product Security and Telecommunications Infrastructure Bill, outlining the problems the Bill will address and how.
How you import from and export to Switzerland.
How to prevent the introduction and spread of animal and bird disease by following good hygiene and biosecurity standards.
Get help to classify footwear and parts of footwear for import and export.
Emerging techniques on how to prevent or minimise the environmental impacts of hydrogen production by electrolysis of water.
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