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Data, Freedom of Information releases and corporate reports
Notifications of COVID-19 and influenza point-of-care testing (POCT) results: legal duties for providers of POCT.
Information and guidance on a range of medical devices for users and patients.
This guide is about infections that occur in people who inject drugs (PWID).
PHE's public health laboratories provide routine and enhanced molecular diagnostic services to NHS trusts.
Information on accessing healthcare for visitors to the UK from EU countries, Norway, Iceland, Liechtenstein and Switzerland.
Find out who can get a free rapid lateral flow test, how to use the test and what your test result means.
This document explains the process for how conditions become part of NHS population screening.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
Supporting health and care professionals to improve services by better understanding the health outcomes that some people in the Roma community face.
Education and training resources for people working in and with UK National Screening Committee-recommended NHS screening programmes in the 4 UK countries.
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
Form D20: Medical examination statement of parties and examiner.
How to use a quasi-experimental study to evaluate your digital health product.
Information on the programme, including commissioning, quality assurance, education and training.
Advice and guidance on the health needs of migrant patients for healthcare practitioners.
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