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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.
Find out if you need an Academic Technology Approval Scheme (ATAS) certificate to study in the UK.
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)’
Information about the EU Regulations and their implementation in Northern Ireland
RA1, RA2, RA3, RA4, RA5 bilingual forms for completion following a drugs test in custody.
Investors and businesses may be legally required to tell the government about certain sensitive acquisitions under the National Security and Investment Act.
Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
How to apply for an authorisation to manufacture authorised veterinary medicines or medicines marketed under the Exemptions for small pet animals.
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.
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.
Guidance for manufacturers, importers and distributors.
The information required by the Regulator of Social Housing and the deadlines for submission.
Sets out when planning permission is required and different types of planning permission which may be granted.
Find the notes for all Declaration Category Data Set tables covered by Appendix 21-25 of the CDS Declaration and Customs Clearance Request Instructions.
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