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Guidance primarily aimed at local responders covering some common issues that may arise during the Recovery Phase of an emergency in the UK.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
A selection of data tables, published alongside the TAG uncertainty toolkit, to help consider and model the common analytical scenarios.
Guidance for manufacturers of artificial heart valves. It outlines specific scenarios that should be considered when determining if an incident is reportable.
Guidance on the collection, verification, and reporting of safety events in clinical trials of an investigational medicinal product.
Explanation for animal owners and veterinary health professionals on how the VMD calculates adverse event incidence rates for veterinary medicines
Guidance for manufacturers of coronary stents. It outlines specific scenarios that should be considered when determining if an incident is reportable.
A resource designed to support policymakers and others in using the Scenarios tool described in the Futures Toolkit.
Advice and guidance on the health needs of migrant patients for healthcare practitioners.
How networks and individuals can support the country's emergency planning, response and recovery, and keep systems and services running.
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