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How you import from and export to Japan.
What you need to do to comply with regulations on manufactured goods you place on the EU market.
Overview of the Data Protection Act
First published during the 2016 to 2019 May Conservative government
This guidance summarises our approach to pharmacovigilance
Details of the organisations that are currently approved to undertake conformity assessments on medical devices.
Use the online service to report non-customs state aid payments you’ve received to HMRC and view your state aid allowance if you’ve claimed customs duty waivers.
How to get state healthcare if you live, work or study in Italy.
What you need to do if you're planning to start higher education in the EU.
Use these general provisions to help you determine the origin of your products.
How to use the procedure for medicines licensing applications.
You can use the bulk import reduced data set to declare one or more low value parcels in a single import declaration when you import goods into Great Britain.
The MHRA will review applications for orphan designation at the time of a marketing authorisation (MA) or variation application.
Information about when you need to submit substantial amendments to a clinical trial including changes to the trial sponsor or legal representative, Investigational medicinal product certification and importation.
This page links to Governments border related Application Programming Interfaces (APIs) which allow industry to integrate their technology with Government systems. This page will be continuously updated as APIs change and ne…
Heavy goods vehicle (HGV) and trailer documents you need to legally cross international borders in a UK-registered vehicle.
Information to help food businesses comply with nutrition legislation.
Check if you can make a declaration by conduct or orally if you’re claiming Returned Goods Relief or Temporary Admission for reusable packaging.
Check if you should pay National Insurance in the UK or social security contributions in the EU, Gibraltar Iceland, Liechtenstein, Norway, or Switzerland.
A checklist for musical artists and accompanying staff working, performing or touring in an EU country, Switzerland, Norway, Iceland or Liechtenstein.
Outlining the principles for the management and oversight of the import of investigational medicinal products (IMPs) to Great Britain from listed countries.
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