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Sets out COVID-19 testing for hospice patients and staff.
Guidance primarily aimed at local responders covering some humanitarian issues that may arise during the recovery phase of an emergency in the UK.
This bulletin presents statistical information on patient education/self management programmes for long term conditions collected from health and social care trusts and independent providers. It details information on the type, provision, frequency and trust area of the programmes delivered.
How to use a before-and-after study to evaluate your digital health product.
What to do if you're appealing or referring someone to appeal a Health, Education and Social Care Chamber (Mental Health) Tribunal decision. (T112)
The independent advisory group identified which patient groups are at highest risk of serious illness from COVID-19 and would benefit from new COVID-19 treatments.
Forms and guidance for professionals working with restricted patients (mentally disordered offenders).
How to use a case-control study to evaluate your digital health product.
Information for healthcare professionals to protect the public from pressure ulcers (bed sores).
Explains testing from 1 April 2024 onwards and sets out the purpose of ongoing testing, who will be eligible to access testing and when tests should be used.
What to do if you're a victim (or family member of a victim) of a violent or sexual offence committed by a person detained under the Mental Health Act. (T118)
How to use a cost benefit analysis to evaluate your digital health product.
Presents statistical information on patient education / self management programmes for long term conditions including information on the type, provision, frequency and trust area of the programmes delivered.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
How investigators and sponsors should manage clinical trials during COVID-19
Advice and guidance on the health needs of migrant patients for healthcare practitioners.
The following guidance has been jointly developed by the Heath Research Authority (HRA) and MHRA, in consultation with the Information Commissioners Office (ICO), on behalf of the UK.
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