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For Internal IRB Use:Institutional Review Board (IRB)IRB Protocol #: Level of Review: Approval Category: Action:IRB Amendment and Report Form U Mass Dartmouth (UMD) requires studies of all approval
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How to fill out irb amendment form v0103
How to fill out irb amendment form v0103
01
Obtain the latest version of the IRB Amendment Form v0103
02
Fill out the general information section including study title, protocol number, PI name, contact information, etc.
03
Clearly state the changes being made to the protocol in specific detail
04
Provide a rationale for the proposed changes
05
Include any necessary supporting documentation (e.g. revised study documents, consent forms, etc.)
06
Obtain all required signatures including PI, co-investigators, and any other relevant parties
07
Submit the completed form to the IRB for review and approval
Who needs irb amendment form v0103?
01
Researchers conducting studies that have already been approved by an Institutional Review Board (IRB) may need to fill out IRB Amendment Form v0103 when modifications to the approved protocol are necessary.
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What is irb amendment form v0103?
The IRB amendment form v0103 is a document used to request changes to an approved research protocol.
Who is required to file irb amendment form v0103?
Researchers conducting studies that have received approval from an Institutional Review Board (IRB) are required to file the IRB amendment form v0103.
How to fill out irb amendment form v0103?
The IRB amendment form v0103 must be filled out with details of the proposed changes to the research protocol, including the rationale for the amendments and any potential risks to participants.
What is the purpose of irb amendment form v0103?
The purpose of the IRB amendment form v0103 is to ensure that any changes to approved research protocols are reviewed and approved by the IRB to protect the rights and safety of research participants.
What information must be reported on irb amendment form v0103?
The IRB amendment form v0103 must include details of the proposed changes, the rationale for the amendments, any potential risks to participants, and any other relevant information.
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