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MISSOURI DEPARTMENT OF HEALTH AND SENIOR SERVICES SUSPECT TULAREMIA CASE INVESTIGATION FORM Today's date: ___/___/___ Patient name Sex: c Male ID :First ___ c Females ___Home address:Date of birth:___/___/___
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Read the instructions provided with the case report form
02
Ensure you have all the necessary information and data before starting to fill out the form
03
Start with the patient information section and fill out all the required details
04
Provide a detailed description of the case history and symptoms
05
Include any relevant laboratory or diagnostic test results
06
Document any treatments or medications administered
07
Fill out the adverse events section if applicable
08
Complete any additional sections or fields as required
09
Review the filled form for accuracy and completeness
10
Submit the completed case report form as instructed or according to the submission guidelines

Who needs case report form?

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Healthcare professionals
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Researchers
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Pharmaceutical companies
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Regulatory authorities
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Clinical trial investigators
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Medical institutions
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Healthcare organizations
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A case report form is a document used in clinical trials to collect data about individual participants.
Investigators and research teams involved in the clinical trial are required to file case report forms.
Case report forms are typically filled out by recording data on paper or electronically, following the instructions provided in the form.
The purpose of a case report form is to collect accurate and reliable data to ensure the safety and efficacy of the trial intervention.
Information such as participant demographics, medical history, adverse events, and treatment outcomes must be reported on a case report form.
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