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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…
Gastrointestinal diseases can be notified using this form.
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.
Antenatal data collection forms for the National Congenital Anomaly and Rare Disease Registration Service (NCARDRS).
Guidelines for managing serious pneumococcal disease in hospitals, care homes, prisons, children’s day-care centres and military settings.
Form for requesting HIV data including: diagnosed individuals receiving HIV care, first HIV and AIDS diagnoses and deaths among HIV positive individuals.
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.
Letter templates to confirm a parent or carer has declined newborn blood spot screening.
For requesting data on sexually transmitted infection (STI) diagnoses and sexual health services provided in England.
For reporting mandatory surveillance of Clostridioides difficile infection to Public Health England.
Expressions of interest for a project which aims to improve people’s mental health through green social prescribing.
Form to help medical practitioners survey suspected cases of salmonella.
Template for child health records departments (CHRD) to collect and submit newborn blood spot screening data.
Form (N1) for submission for culture, identification and sensitivities.
Form and guidelines for authors applying to publish in the 'Chemical hazards and poisons (CHaP) report'.
Postnatal data collection forms for the National Congenital Anomaly and Rare Disease Registration Service (NCARDRS).
Coronavirus (COVID-19) vaccination consent forms and letter templates for use by GPs, the NHS or healthcare and social care employer organisations.
Combined Review Forms (CRF) for community treatment services to use for Core Dataset P (CDS-P), from April 2020 onwards.
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