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Guidance and resources to resolve common fingermark visualisation queries and help forensic laboratories achieve and maintain ISO 17025.
Guidance for practitioners involved in the recovery of evidential fingermarks.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
This playbook explains how we use social media at GDS. In it, we share our best practice, what we've learned and what we're planning to do.
The second edition of the Fingermark Visualisation Manual will help forensic practitioners maximise fingermark recovery and aid criminal investigations.
Advice on carrying out fingermark visualisation processes on receipts produced on paper that releases bubbles of ink when heated.
Advice and guidance on the health needs of migrant patients for healthcare practitioners.
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
Information to help healthcare professionals make decisions about the planning and provision of services using child and maternal health data and intelligence.
Newletters providing updates for the forensic community in support of the Fingermark Visualisation Manual since 2003.
Information about the EU Regulations and their implementation in Northern Ireland
This page collates the various existing ethical principles for data and AI, developed by government and public sector sector bodies. It intends to provide clarity and guidance for public servants working with data and/or AI.
Links to EU guidance, as it stood immediately before end of transition period.
Information and guidance on a range of medical devices for users and patients.
How to show MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
Advice for medical professionals to follow when assessing drivers with neurological disorders.
How to arrange an effective external review of governance and improve the performance of your board.
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.
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