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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.
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...
Information about the EU Regulations and their implementation in Northern Ireland
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)’
Investors and businesses may be legally required to tell the government about certain sensitive acquisitions under the National Security and Investment Act.
Find out if you need an Academic Technology Approval Scheme (ATAS) certificate to study in the UK.
RA1, RA2, RA3, RA4, RA5 bilingual forms for completion following a drugs test in custody.
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
How to carry out a flood risk assessment so that you can complete your planning application.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Resources supporting the Government Functional Standard for Property (GovS 004).
How UK nationals who plan to live in Spain for more than 3 months must register as a resident and on the padrón at their town hall.
What we require from each different type of landlord and the approach we will take
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
How to make sure that your products are properly checked for conformity and your technical documents are managed correctly.
Guidance for manufacturers, importers and distributors.
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