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FOR IRB USE ONLY IRB ID #: 201910191 APPROVAL DATE: 01/28/20 RELEASED DATE: 01/29/20 EXPIRATION DATE: 11/25/20INFORMED CONSENT DOCUMENT Project Title: Postpartum depression after Cesarean delivery:

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Researchers conducting studies that require IRB approval need IRB ID 201910191.

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What is irb id 201910191?

irb id 201910191 is the unique identifier assigned to a specific Institutional Review Board (IRB) protocol.

Who is required to file irb id 201910191?

The principal investigator or researcher responsible for the study is required to file irb id 201910191.

How to fill out irb id 201910191?

To fill out irb id 201910191, the researcher must provide detailed information about the study protocol, including the study design, objectives, methods, and risk mitigation strategies.

What is the purpose of irb id 201910191?

The purpose of irb id 201910191 is to ensure that research involving human subjects is conducted ethically and in compliance with regulatory requirements.

What information must be reported on irb id 201910191?

Information that must be reported on irb id 201910191 includes the study protocol, informed consent forms, data collection procedures, and any potential risks to participants.

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