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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 import plants, fruit, vegetables, cut flowers, trees, seeds and used agricultural machinery to Great Britain (England, Scotland and Wales) from the EU, Liechtenstein and Switzerland.
Advice and support for those who are experiencing or feel at risk of sexual violence and abuse.
How to use a risk-based approach to carry out compulsory risk assessments of your business.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
How the MHRA makes decisions on when a product is a medical device (borderline products), and which risk class should apply to a medical device.
Advice for medical professionals to follow when assessing drivers with neurological disorders.
Sign up to HM Land Registry's free Property Alert service to help protect your property from fraud.
Organisational definitions of terms concerned with risk and risk-related matters.
Information for UK businesses on political, economic and security risks when trading overseas.
These reports explain our assessment of the scientific evidence used to lead to regulatory decisions on the safety of medicines or medicines classes.
Housing options and support for veterans who are homeless or at risk of becoming homeless
How to import animals and animal products to Great Britain (England, Scotland and Wales), the Channel Islands and the Isle of Man from non-EU countries.
Explains testing from 1 April 2024 onwards and sets out the purpose of ongoing testing, who will be eligible to access testing and when tests should be used.
FCDO travel advice for St Kitts and Nevis. Includes safety and security, insurance, entry requirements and legal differences.
Check if you need to apply for an environmental permit, formerly known as a flood defence consent, and get the forms you need.
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
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