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How a product complies with EU safety, health and environmental requirements, and how to place a CE marking on your product.
The conditions that new cemetery developments, or new extensions of a cemetery, can operate under without needing an environmental permit.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
Labelling rules for businesses in Great Britain (England, Scotland and Wales) and retailers in Northern Ireland, for certain agri-food products moved under the Northern Ireland Retail Movement Scheme.
Investors and businesses may be legally required to tell the government about certain sensitive acquisitions under the National Security and Investment Act.
Local plan examinations and the planning issues they deal with can be complex. This is intended as a short guide for those who might be participating in a local plan examination for the first time. It does not aim to...
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
How to carry out a flood risk assessment so that you can complete your planning application.
Guidance for manufacturers, importers and distributors.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
Guidance on the European Union regulation on explosives precursors, including licensing, labelling and reporting suspicious activity
Advice for state-funded school admission authorities, independent schools, local authorities and parents.
General advice for conveyancers on how to avoid requisitions.
A wholesale dealer in Great Britain may import Qualified Person certified medicines from the European Economic Area if certain checks are made by the ‘Responsible Person (import)’
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
How to make sure that your products are properly checked for conformity and your technical documents are managed correctly.
Explains planning controls relating to the storage of hazardous substances in England and how to handle development proposals around hazardous establishments.
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