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The Medicines and Healthcare products Regulatory Agency (MHRA) has today (6 March 2024) approved the Rubidium (Rb82) Generator (RUBY-FILL) as a diagnostic tool for imaging of the heart, to evaluate blood flow and aid in the diagnosis or assessment of...
Quick reference materials for primary care on diagnosing and understanding culture results for urinary tract infections (UTI).
Advice for manufacturers, members of the public and professional users of software or apps being used during the COVID-19 pandemic.
This guide is intended for all plant doctors and other plant health advisors around the world
And other trematode infections in wildlife reservoirs
Quality assurance and control (QA/QC) is an essential element of a breeding program’s optimization efforts towards increased genetic gains
Information for manufacturers, healthcare organisations and professionals, researchers, and patients & public on Software as a Medical Device (SaMD), including Artificial Intelligence as a Medical Device (AIaMD).
This document explains the Down’s syndrome screening quality assurance support service (DQASS) and how to use it.
This procurement diagnostic tool allows you to immediately identify your procurement strengths and weaknesses, and explains how to improve procurement to make savings.
Information on when software applications are considered to be a medical device and how they are regulated.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
The Republic of Kiribati, Central Pacific, has the largest tuberculosis epidemic in the region
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