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Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
How to use a cost utility analysis to evaluate your digital health product.
How we engage and involve patients and the public in our regulatory decision-making.
Find out what unacceptable or unreasonable actions are and how we approach them.
If you import into or export from Northern Ireland you can get a decision on the origin of your goods.
How to use a cost consequence analysis to evaluate your digital health product.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
FCDO travel advice aims to inform British nationals so they can make decisions about travelling abroad. This page sets out how the FCDO assesses risks and compiles travel advice.
How to write up and share your findings
Sets out the process for efficient and inclusive consultation of planning applications
How to hold charity trustee and member meetings, including AGMs, so you can make decisions legally and your charity can run effectively.
The Regulations place a duty on railway industry bodies (infrastructure managers, railway operators, or maintainers), involved in an accident or incident, to notify us.
Sets out the role and approach of the DSA to improve the adoption of common data standards across government over the next 3 years.
How to use an economic evaluation to evaluate your digital health product.
This information is provided to help British nationals make decisions about getting medical advice and reporting a rape or sexual assault in Russia.
How we evaluated pre-exposure prophylactic (preventative) treatments for COVID-19.
Compare different evaluation approaches and choose an appropriate method.
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