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Guidance to help organisations choose a monitoring approach for stack emissions to air that meets Environment Agency and MCERTS requirements (formerly part of M2).
Check the regulations on aircraft parts imported with a certificate of airworthiness.
Check how much your visa application costs in the country you’re in
Look up a trade mark to see if something identical or similar to your brand is already registered.
Applications received to amend the specification of a patent under sections 27 and 75 before the court and the Office.
Listing of countries with a known occurrence of high consequence infectious disease (HCID).
When tests to detect COVID-19 are commonly used (use cases) and what to consider when deciding which type of test to employ.
Find out if you need an Academic Technology Approval Scheme (ATAS) certificate to study in the UK.
Use this form to file a translation in connection with a European patent or a European patent application
Protocols and procedures for testing the distinctiveness, uniformity and stability (DUS) of certain agricultural and vegetable plants.
Check the tariff classification for articles made of cermet.
Get help to classify pharmaceutical products used to treat or prevent diseases or ailments (in humans or animals), including comparators used in clinical trials and placebos.
How UK private maritime security companies (PMSCs) get sealed and signed physical certificates to meet documentation requirements of overseas governments.
This guidance specifies the standards for the continuous monitoring and sampling of stack emissions.
Examples of how and when to adjust the customs value for commercial level and quantity when using Methods 2 or 3 if you’re an importer or clearing agent.
How to object to the registration of a lasting or enduring power of attorney - including forms and fees
Advice for medical professionals to follow when assessing drivers with neurological disorders.
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
This page provides practical information to help you make the most of your IP when doing business in Peru.
Guidance for organisations involved in any aspect of the pharmaceutical lifecycle or GLP studies regulated by MHRA, covering the approval of paper documents when working from home
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