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The different types of tests and testing kits for COVID-19, and the specifications for manufacturers.
The Diagnostic Imaging Dataset (DID) is a central collection of detailed information about diagnostic imaging tests carried out on NHS patients, extracted from local Radiology Information Systems (RISs) and submitted monthly. The DID captures information about referral source and patient...
Information for pregnant women who are offered a chorionic villus sampling (CVS) or amniocentesis diagnostic test.
Guidance on raising performance concerns when a coronavirus (COVID-19) test product is impacted by a variant of concern (VOC) or other emerging variant (V).
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Guidance on who to test for Zika virus infection and which samples to collect.
Use these log sheets to record and review equipment use in local Newborn Hearing Screening Programmes (NHSP).
Community diagnostic centre (CDC) sites have already delivered over 7 million tests, checks and scans to patients across England.
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
How to show MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
Good Practice Guide (GPG) 45 helps you decide how to check someone's identity.
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
Information about the EU Regulations and their implementation in Northern Ireland
Weights and Measures Act 1985 and subsequent Deregulation Order 1999 (as amended).
Diagnostic request form (S3) for HIV.
Information for health professionals on the epidemiology, transmission and prevention of Chlamydia abortus which can cause stillbirth or abortion in humans.
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