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NORTHERN CONGENITAL ABNORMALITY SURVEY (Dorcas)
SURVEY OF FETAL ABNORMALITY AND CONGENITAL MALFORMATION IN THE NORTH EAST AND NORTH CAMBRIA
Survey Coordinator (Ms Mary Bothell), Maternity Survey
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Remember that the norformrn congenital abnormality survey is typically required for individuals who have a family history of congenital abnormalities, are pregnant, or have other relevant medical conditions. It is important to consult with your healthcare provider to determine if you need to fill out this survey.
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What is norformrn congenital abnormality survey?
Norformrn congenital abnormality survey is a survey that collects data on congenital abnormalities in newborns.
Who is required to file norformrn congenital abnormality survey?
Healthcare providers and hospitals are required to file norformrn congenital abnormality survey.
How to fill out norformrn congenital abnormality survey?
The survey can be filled out online on the designated platform, providing accurate information about newborns with congenital abnormalities.
What is the purpose of norformrn congenital abnormality survey?
The purpose is to gather data for research, monitoring trends, and improving healthcare services for newborns with congenital abnormalities.
What information must be reported on norformrn congenital abnormality survey?
Information such as the type of abnormality, date of birth, gender, and any relevant medical history must be reported on the survey.
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