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Departments, agencies and public bodies
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
A summary of recent letters and notifications sent to healthcare professionals about medicines and medical devices.
How to use a randomised controlled trial to evaluate your digital health product.
Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
Spreadsheets are a common way to share data. Use this information to help you avoid common errors, improve interoperability and create more accessible spreadsheets.
Guidance on how to license electronic cigarettes and other inhaled nicotine-containing products (NCPs) as medicines in the UK.
The epidemiology, symptoms, diagnosis and management of plague.
Information on the reporting, investigation and management of acute flaccid paralysis (AFP) and acute flaccid myelitis (AFM).
Public health principles for reducing the spread of respiratory infections, including COVID-19, in the workplace.
Patient summary form for health professionals to report cases of acute flaccid paralysis (AFP) and acute flaccid myelitis (AFM).
How to write up and share your findings
Find out which birds and animals may be spared from culling during an outbreak of an exotic animal disease.
Find out if you need an Academic Technology Approval Scheme (ATAS) certificate to study in the UK.
Form to report patients meeting the case definition.
Find out how to do a rapid lateral flow test for COVID-19. Rapid lateral flow tests show the result on a device that comes with the test.
When tests to detect COVID-19 are commonly used (use cases) and what to consider when deciding which type of test to employ.
Information for clinicians and patients.
You must tell DVLA if you have a brain abscess, cyst or encephalitis - download the correct form to let them know
How to use A/B testing to evaluate your digital health product.
Use form C88 (status) as proof of authorisation to import or export for the country of destination.
Compare different evaluation approaches and choose an appropriate method.
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