Get the free Protocol Closure Form - research binghamton
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This form is to be completed when a human subjects research project is completed or ends for any reason, ensuring compliance with university and federal regulations regarding human subjects research.
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How to fill out protocol closure form
How to fill out Protocol Closure Form
01
Start by entering the project title at the top of the form.
02
Provide the principal investigator's name and contact information.
03
Fill in the protocol number assigned to your study.
04
Indicate the date of study completion or termination.
05
Summarize the main findings of the study in the designated section.
06
List any publications or presentations that resulted from the study.
07
Provide an explanation for the closure of the protocol, if applicable.
08
Sign and date the form to certify that the information provided is accurate.
Who needs Protocol Closure Form?
01
The principal investigator and research team members.
02
Institutional Review Board (IRB) members.
03
Funding agencies or sponsors of the study.
04
Regulatory bodies overseeing clinical trials.
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What is Protocol Closure Form?
The Protocol Closure Form is a document used to formally close a research protocol, indicating that the study has been completed or terminated.
Who is required to file Protocol Closure Form?
The principal investigator or the authorized individual responsible for the research study is required to file the Protocol Closure Form.
How to fill out Protocol Closure Form?
To fill out the Protocol Closure Form, provide the required details including the study title, protocol number, completion date, reasons for closure, and any final outcomes of the study.
What is the purpose of Protocol Closure Form?
The purpose of the Protocol Closure Form is to officially document the end of a research project, ensuring compliance with regulatory requirements and allowing for proper record-keeping.
What information must be reported on Protocol Closure Form?
The information that must be reported includes the protocol title, protocol number, closure date, summary of results, and any adverse events or significant findings that occurred during the study.
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