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IRB Number MedStar Health Research Institute-Georgetown University IRB Protocol Review Form for Reviewers PI Name Title of Protocol Reviewer Reviewer Please check the following sections and detail all changes to be made below. Type of Review check one Recommendation check one Full Board Initial Review Approve as submitted Full Board Reactivation Approvable pending minor changes Expedited Initial Review Defer until next meeting Disapprove If expedited list appropriate category below by For...
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What is medstar irb form?
The MedStar IRB form is a document used to request approval for research involving human subjects at MedStar Health facilities.
Who is required to file medstar irb form?
Researchers and investigators conducting research involving human subjects at MedStar Health facilities are required to file the MedStar IRB form.
How to fill out medstar irb form?
To fill out the MedStar IRB form, researchers need to provide detailed information about their research objectives, study design, participant recruitment, informed consent process, data management, potential risks and benefits, and other relevant details.
What is the purpose of medstar irb form?
The purpose of the MedStar IRB form is to ensure that research involving human subjects meets ethical and regulatory standards, protects participant rights and welfare, and obtains necessary approvals before initiating the study.
What information must be reported on medstar irb form?
The MedStar IRB form requires researchers to report information such as study objectives, participant characteristics, study procedures, data collection methods, potential risks and benefits, provisions for informed consent, privacy and confidentiality measures, and any conflicts of interest.
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