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Use supplementary pages SA101 to record less common types of income, deductions and tax reliefs on your SA100 Tax Return.
Guidance on imports from Russia and Belarus requiring additional duties and terms of exemption.
Supports effective delivery of planning application process.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
When applying for Business e-services, use this form to provide details of additional administrators.
UK Shared Prosperity Fund additional information for use by partners.
How to amend or cancel simplified frontier declarations, C21s and non-special procedure non-monetary supplementary declarations.
Sets out special provisions for Crown development for dealing with security-sensitive information in planning applications.
Provides detailed information on both potential types of information and evidence, and the correct way to process and record such information.
Find out the rules from 1 January 2018 if you promote or use arrangements that are meant to give someone a VAT or other indirect tax saving or a tax deferral.
Find out details of the procedure codes and additional procedure codes that are excluded from use with Simplified Declaration Procedure (SDP) with regular use and Entry in Declarants Records (EIDR).
Follow these steps to take when preparing to make a BIRDS declaration or Customs Clearance Request on the Customs Declaration Service..
What to do if you think you are a victim of identity theft or fraud, and what signs to look out for.
This guidance provides information about permission in principle - a new planning consent route.
Follow these steps to when preparing to make a Final Supplementary declaration (FSD) on the Customs Declaration Service.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Find codes for the additions or deductions to the item price or amount being declared in the Customs Declaration Service (Appendix 10).
There are different regulations which apply to devices and equipment including hand gels and PPE (personal protective equipment)
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.
How to show MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
Don’t include personal or financial information like your National Insurance number or credit card details.
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