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News stories, speeches, letters and notices
Detailed guidance, regulations and rules
Reports, analysis and official statistics
Consultations and strategy
Data, Freedom of Information releases and corporate reports
Advice and guidance on the health needs of migrant patients for healthcare practitioners.
Safety leaflet on topical corticosteroids and withdrawal reactions to help patients and their carers to use these medicines safely.
You must tell DVLA if you have been fitted with a pacemaker - download the correct form to let them know
Information for patients, healthcare professionals and the wider public to help better understand the importance of AAIs as a potential life-saving medicine.
This guidance explains what rules of origin (RoOs) are and the changes under the Developing Countries Trading Scheme (DCTS).
Project Orbis is a programme to review and approve promising cancer drugs helping patients access treatments faster.
An overview of capital funding for post-16 education providers, the type of funding available, what it can be used for and when to apply.
These reports explain our assessment of the scientific evidence used to lead to regulatory decisions on the safety of medicines or medicines classes.
Guidance for the pharmaceutical industry on Marketing Authorisations for veterinary medicines.
This guide is about infections that occur in people who inject drugs (PWID).
Information for companies on the import and export of controlled drugs to and from the UK.
Guidance for schools on creating a policy around the use of emergency auto-injectors (AAI)
Neon Healthcare Ltd is recalling the specific batch mentioned in this notification as a precautionary measure.
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
This series brings together all documents relating to Guidance and methods
An independent tribunal responsible for handling appeals against decisions made by the Secretary of State for Health and Social Care from pharmaceutical companies.
Search for information about medicines including patient information leaflets (PILs), details on how the medicine can be used (SmPCs) and scientific reports (PARs).
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.
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