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Pediatric pulmonary thromboembolism CANADIAN Pediatric SURVEILLANCE PROGRAM 1002305 St. Laurent Blvd. Ottawa, ON K1G 4J8 Tel: 6135269397, ext. 239 Fax: 6135263332 cpsp@cps.ca www.cpsp.cps.caREPORTING
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How to fill out canadian paediatric surveillance program
How to fill out canadian paediatric surveillance program
01
Contact the Canadian Paediatric Society to obtain a registration form for the program
02
Fill out the registration form with your contact information and any relevant credentials
03
Submit the completed registration form to the CPS for review and approval
04
Once approved, you will receive further instructions on how to report paediatric cases to the surveillance program
Who needs canadian paediatric surveillance program?
01
Healthcare professionals who work with children and are involved in paediatric care
02
Researchers studying childhood illnesses and diseases
03
Public health officials tracking trends in paediatric health
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What is canadian paediatric surveillance program?
The Canadian Paediatric Surveillance Program (CPSP) is a national active surveillance program that monitors the incidence and prevalence of rare and serious paediatric diseases and conditions.
Who is required to file canadian paediatric surveillance program?
Health care professionals, such as paediatricians, child health specialists, and other physicians, are required to file reports to the Canadian Paediatric Surveillance Program.
How to fill out canadian paediatric surveillance program?
Health care professionals can fill out the Canadian Paediatric Surveillance Program by submitting reports online through the CPSP website or by mail using the provided reporting forms.
What is the purpose of canadian paediatric surveillance program?
The purpose of the Canadian Paediatric Surveillance Program is to facilitate the early detection of rare and serious paediatric diseases, to monitor their trends over time, and to inform public health decision-making.
What information must be reported on canadian paediatric surveillance program?
Health care professionals must report detailed information about cases of rare and serious paediatric diseases, including patient demographics, diagnosis, treatment, and outcomes.
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