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Version 6/12/2019 IRB # 7657 CTI Feasibility Pilot Consent Reinformed Consent for Participation in Research Adapting Critical Time Intervention to Support Inpatient Medical Care Transitions Sponsor:
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How to fill out protocol summary form 7657
How to fill out protocol summary form 7657
01
To fill out protocol summary form 7657, follow these steps:
02
Start by providing the title of the protocol in the designated field.
03
Enter the date when the protocol was initiated.
04
Provide a brief summary of the protocol, mentioning the objectives and key procedures.
05
Indicate the names and roles of all individuals involved in conducting the protocol.
06
Include any necessary references or citations related to the protocol.
07
Review the form for accuracy and completeness.
08
Finally, sign and date the form to certify its completion.
Who needs protocol summary form 7657?
01
Protocol summary form 7657 is needed by researchers, scientists, or anyone involved in conducting experiments or studies that require a formal summary of the protocol followed. It serves as a documentation tool to outline the key aspects of the protocol and ensure proper communication and understanding among relevant parties.
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What is protocol summary form 7657?
Protocol summary form 7657 is a document that outlines the key details of a research protocol.
Who is required to file protocol summary form 7657?
Researchers conducting clinical trials are required to file protocol summary form 7657.
How to fill out protocol summary form 7657?
Protocol summary form 7657 can be filled out online by providing information about the research protocol, study objectives, methodology, and anticipated outcomes.
What is the purpose of protocol summary form 7657?
The purpose of protocol summary form 7657 is to provide regulatory authorities with an overview of the research protocol to ensure transparency and compliance with regulations.
What information must be reported on protocol summary form 7657?
Protocol summary form 7657 requires information such as the study title, principal investigator, study design, patient eligibility criteria, and study endpoints.
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