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Search for information about medicines including patient information leaflets (PILs), details on how the medicine can be used (SmPCs) and scientific reports (PARs).
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
How to access the historical censuses from 1841 to 1921.
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
Explains how commissioners and health professionals can use data and analysis for decisions about dementia services and interventions.
Templates and legal documents to help you buy and supply G-Cloud services.
This collaboration offers a strategic opportunity for the UK and ROK to establish global leadership in the priority area of Open RAN network power efficiency.
Examples of viral haemorrhagic fevers (VHFs) include Lassa fever, Crimean-Congo haemorrhagic fever, Marburg and Ebola virus diseases.
The MHRA will introduce a patient alert card to increase awareness among men taking finasteride about potential psychiatric and sexual side effects
These are the main documents relating to the Building Safety Bill.
Find out about the long-term effects some people can have after having COVID-19.
A brief explainer of some of the key policy areas of the Prisons Strategy White Paper.
Statement by UK Spokesperson to the UN Mungo Woodifield at the UN Committee on Information General Debate.
How to come back to the UK to live if you were previously settled (given indefinite leave to remain) - find out if you need a Returning Resident visa
Monitor the progress of a patent application through search reports, open to the public inspection files, and caveats.
This page brings together government's work and announcements on loneliness.
How responders can reduce the risk of communications disruption during emergencies by using ResilienceDirect, HITS and Telecoms Sub-Groups.
Information about when you need to submit substantial amendments to a clinical trial including changes to the trial sponsor or legal representative, Investigational medicinal product certification and importation.
Instructions on how members of the public can submit their submissions to support the work of the team of experts leading the review.
Advice on exposure to electromagnetic fields in the everyday environment, including electrical appliances in the home and mobile phones.
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