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Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
Guidance to help you develop a business continuity plan
This guidance provides information on COVID-19 in homelessness, domestic abuse refuge, respite room and asylum seeker accommodation settings.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
FCDO travel advice for the Dominican Republic. Includes safety and security, insurance, entry requirements and legal differences.
Find out what unacceptable or unreasonable actions are and how we approach them.
Qualified Persons (QPs) should follow the below guidance on the flexible approaches we are taking for medicines imported from third countries.
National review into sudden unexpected death in infancy in families where children are considered at risk of significant harm.
How investigators and sponsors should manage clinical trials during COVID-19
How to export or move fish for human consumption from the UK.
Information on the role of the Home Office Forensic Pathology Unit and its support of the Pathology Delivery Board.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
Find out if you can make a late claim if you’ve missed the deadline and how to do this. You can also check guidance for the scheme.
Guidance for industry on flexible approaches we are taking on good distribution practices.
Find out what repairs or processing you can do to your goods in a customs warehouse without authorisation, this is known as usual forms of handling.
Guidance about cost of living related financial difficulties in charities.
Check what to do after a death - how to register the death, notify government departments and deal with the estate.
This guide is the result of a unique partnership between the business community, police and business continuity experts.
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