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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鈥�
The FOQ is mandatory for all antenatal booking blood requests submitted in鈥�
Coronavirus (COVID-19) vaccination consent forms and letter templates for care home residents.
Coronavirus (COVID-19) vaccination consent form and letter templates for adults who are able to consent.
Guidelines for managing serious pneumococcal disease in hospitals, care homes, prisons, children鈥檚 day-care centres and military settings.
Gastrointestinal diseases can be notified using this form.
Antenatal data collection forms for the National Congenital Anomaly and Rare Disease Registration Service (NCARDRS).
For reporting mandatory surveillance of Escherichia coli bacteraemia, Klebsiella species and Pseudomonas aeruginosa to Public Health England.
Request form P4 to accompany Zika (no current symptoms) samples sent to the Rare and Imported Pathogens Laboratory.
Form to help medical practitioners survey suspected cases of salmonella.
For reporting mandatory surveillance of Staphylococcus aureus bacteraemia to Public Health England.
Letter templates to confirm a parent or carer has declined newborn blood spot screening.
Invite expectant fathers for sickle cell and thalassaemia screening when the mother carries an unusual haemoglobin gene.
Form and guidelines for authors applying to publish in the 'Chemical hazards and poisons (CHaP) report'.
Delivery data collection forms for the National Congenital Anomaly and Rare Disease Registration Service (NCARDRS).
Use this form to submit research requests to the NHS abdominal aortic aneurysm (AAA) screening programme, for research involving patients or their data.
Coronavirus (COVID-19) vaccination consent forms and letter templates for use by GPs, the NHS or healthcare and social care employer organisations.
Maternity unit data return form and laboratory data return form for data from 1 April 2016 to 31 March 2017.
Postnatal data collection forms for the National Congenital Anomaly and Rare Disease Registration Service (NCARDRS).
Forms for reporting cases of acute hepatitis A, acute hepatitis B and acute hepatitis C diagnosed in Genitourinary Medicine Clinics (GUM) to local health protection teams (HPTs).
Template for child health records departments (CHRD) to collect and submit newborn blood spot screening data.
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