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Use form C&E48 to apply for authorisation to use simplified procedures for importing and exporting.
Choose how you’ll make supplementary declarations for goods that you entered into your own records without authorisation.
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.
Guidance for the pharmaceutical industry on how to apply to vary a veterinary Marketing Authorisation (MA) or Homeopathic Remedy.
Lists of standards that businesses can use to show their products, services or processes comply with essential requirements of legislation.
The European Trade Mark and Design Network has produced a common practice for use when assessing the inherent distinctiveness of figurative trade marks containing descriptive and/or non-distinctive words.
How the MHRA processes variations to Marketing Authorisations (MAs)
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.
Standardisation explained.
Find out about customs special procedures and outward processing that allow you to suspend, pay less or pay no duty on goods you import or export.
Guidance for industry on flexible approaches we are taking on good distribution practices.
Depending on the objection raised in your examination, you have 2 months to respond through a number of options.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
Helping public health practitioners conducting evaluations – developing a logic model to represent how your intervention works.
Explanation of legal phrases used in the Civil Procedure Rules.
Find out what repairs or processing you can do to your goods in a customs warehouse without authorisation, this is known as usual forms of handling.
Find out about other simplifications you can apply for with consignor or consignee status.
Find out what rights and obligations you can transfer, if you can transfer or receive them and what to do after authorisation.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
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