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APPENDIX Principal Investigator Responsibilities to the MRECWelcome to the Franciscan Health System Medical Research Evaluation Committee (REC). As a Principal Investigator (PI) you are responsible
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How to fill out investigator flow sheet template

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How to fill out investigator flow sheet

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Step 1: Start by gathering all necessary information about the investigation.
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Step 2: Identify the key questions and objectives of the investigation.
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Step 3: Fill out the basic details section of the investigator flow sheet, including the date, case number, and investigator's name.
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Step 4: Begin documenting the case details, including the nature of the incident, involved parties, and any witnesses.
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Step 5: Use a point-by-point approach to outline specific steps taken during the investigation, including interviews, evidence collection, and analysis.
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Step 6: Document any findings, observations, or conclusions made during the investigation.
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Step 7: Ensure all relevant information is accurately recorded, including dates, times, and descriptions of events.
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Step 8: Review the completed investigator flow sheet for accuracy and completeness before submitting.

Who needs investigator flow sheet?

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Any individual or organization seeking a structured and organized approach to documenting investigative processes.

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An investigator flow sheet is a document used to track the progress and activities of an investigator in a research study or clinical trial, ensuring that all necessary data and compliance measures are adequately recorded.
Typically, the principal investigator or research staff involved in clinical trials or research studies are required to file the investigator flow sheet.
To fill out an investigator flow sheet, you should provide relevant details such as participant enrollment dates, data collection methods, visit dates, adverse events, and any necessary regulatory compliance information as outlined in the trial protocol.
The purpose of the investigator flow sheet is to maintain accurate records of study-related activities, ensure compliance with regulatory requirements, and provide a comprehensive overview of the study's progress.
Information that must be reported includes participant demographics, enrollment dates, visits, data collection efforts, adverse events, and any deviations from the study protocol.
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