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Detailed guidance, regulations and rules
Reports, analysis and official statistics
Consultations and strategy
Data, Freedom of Information releases and corporate reports
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
Investors and businesses may be legally required to tell the government about certain sensitive acquisitions under the National Security and Investment Act.
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.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Guidance for manufacturers, importers and distributors.
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)’
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.
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
General advice for conveyancers on how to avoid requisitions.
Legal requirements and good practice guidance for SQP retailers’ premises inspections.
Explains planning controls relating to the storage of hazardous substances in England and how to handle development proposals around hazardous establishments.
Explains how conditions attached to a planning permission should be used and discharged effectively
What we require from each different type of landlord and the approach we will take
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
Sets out when planning permission is required and different types of planning permission which may be granted.
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
Guidance on the content of a Development Consent Order required for a Nationally Significant Infrastructure Project.
What you need to know and do to export or import objects of cultural interest.
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