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Essential elements for implementation of the family origin questionnaire (FOQ) to help assess if a person is a likely carrier for sickle cell and thalassaemia (SCT).
The family origin questionnaire (FOQ) is mandatory for all antenatal…
The FOQ is mandatory for all antenatal booking blood requests submitted in…
Coronavirus (COVID-19) vaccination consent forms and letter templates for care home residents.
Guidelines for managing serious pneumococcal disease in hospitals, care homes, prisons, children’s day-care centres and military settings.
Coronavirus (COVID-19) vaccination consent form and letter templates for adults who are able to consent.
For reporting mandatory surveillance of Escherichia coli bacteraemia, Klebsiella species and Pseudomonas aeruginosa to Public Health England.
Antenatal data collection forms for the National Congenital Anomaly and Rare Disease Registration Service (NCARDRS).
Form to help medical practitioners survey suspected cases of salmonella.
Expressions of interest for a project which aims to improve people’s mental health through green social prescribing.
Enhanced surveillance questionnaire for newly diagnosed acute hepatitis B cases
For reporting mandatory surveillance of Staphylococcus aureus bacteraemia to Public Health England.
Gastrointestinal diseases can be notified using this form.
Coronavirus (COVID-19) vaccination consent forms and letter templates for use by GPs, the NHS or healthcare and social care employer organisations.
Use this form to submit research requests to the NHS abdominal aortic aneurysm (AAA) screening programme, for research involving patients or their data.
Form and guidelines for authors applying to publish in the 'Chemical hazards and poisons (CHaP) report'.
HPV school level data collection tools and user guide.
Letter templates to confirm a parent or carer has declined newborn blood spot screening.
These forms are for GPs or other clinicians to fill out, to follow up cases of invasive haemophilus influenzae disease.
For reporting mandatory surveillance of Clostridioides difficile infection to Public Health England.
Postnatal data collection forms for the National Congenital Anomaly and Rare Disease Registration Service (NCARDRS).
Use this form to record and submit data to the Sloane Project.
Don’t include personal or financial information like your National Insurance number or credit card details.
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