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Departments, agencies and public bodies
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Data, Freedom of Information releases and corporate reports
A summary of recent letters and notifications sent to healthcare professionals about medicines and medical devices.
Guidance and support on coronavirus (COVID-19) in Wales.
Information about the EU Regulations and their implementation in Northern Ireland
Find out who can get a free rapid lateral flow test, how to use the test and what your test result means.
How to get fast-track approval of medical devices during COVID-19.
The epidemiology, symptoms, diagnosis and management of plague.
Information on variants of the SARS-CoV-2 virus.
How to use a combination of quantitative and qualitative data to evaluate your digital health product.
Past and current clinical trials into therapeutic and antiviral treatments for COVID-19, how to take part, and which treatments have proven to be effective.
Information and guidance on a range of medical devices for users and patients.
This document explains: how patients are tested and treated, and steps in place to prevent its spread.
Advice on writing clear notices and maximising replies to your FSNs.
Information on the reasons behind human infectious disease emergence, including a timeline and a global map.
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.
Information on COVID-19, including guidance on the assessment and management of suspected UK cases.
Advice and guidance on the health needs of migrant patients from Colombia for healthcare practitioners.
The Scientific Advisory Committee on the medical implications of less-lethal weapons (SACMILL) provides independent advice to UK government departments and organisations on the biophysical, biomechanical, pathological and clinical aspects of less-lethal weapon systems. SACMILL is an advisory non-departmental public body,...
There are different regulations which apply to devices and equipment including hand gels and PPE (personal protective equipment)
Actions that trial sponsors should consider to build resilience into clinical trial design
Advice and guidance on the health needs of migrant patients from Argentina for healthcare practitioners.
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