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Get help to classify ceramic articles for import and export.
Get relief if you’re importing biological and chemical substances for research purposes from outside the EU and UK.
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.
Get help to classify cigarettes, cigars, raw tobacco, smoking tobacco, tobacco for heating and nicotine substitutes for import and export.
These guidelines set out how we examine patent applications for chemical inventions
Rules for local authorities to follow when registering a premises to produce bottled drinking water, or carrying out ongoing checks.
Explains planning controls relating to the storage of hazardous substances in England and how to handle development proposals around hazardous establishments.
List of controlled goods that follow the normal import declaration rules if HMRC apply continuity plans due to system issues.
End-user undertaking form which must be completed as part of the application for a standard individual export licence (SIEL).
How the UK government and devolved governments propose to work together on chemicals and pesticide policies and regulation.
How product specific rules are used to identify the country of origin when importing or exporting between the UK and EU.
Controlled drugs and precursor chemicals licensing fees information for individuals and companies.
How to register as a spring water producer, and the rules you must follow to produce and market spring water.
Class and permitted use of passenger ships, cargo ships, tankers, tugs, tenders, fishing boats, yachts, commercial vessels, and the required certificates.
Advice and guidance on the health needs of migrant patients for healthcare practitioners.
This document (RCE-3) presents the conclusions of a review of the basis for establishing health-based protection criteria in the areas of chemicals, ionising radiation, and non-ionising radiation.
What kinds of vessels get expanded inspections by the MCA, what happens during the inspections, notice, and where you can find more advice.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
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