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Appendix 4
Participant Informed Consent Form
Protocol Study number: ___
Patient identification number for this study: ___
Title of the project: ___Name of Principal investigator: ___ Mobile No. ___
The
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Who needs annexure 4 participant informed?
01
Researchers conducting clinical trials or studies requiring informed consent from participants.
02
Medical professionals or institutions obtaining consent from patients for specific treatments or procedures.
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What is annexure 4 participant informed?
Annexure 4 Participant Informed is a document used to provide information about participants involved in a specific study or project, ensuring their informed consent and understanding of the study's purpose and procedures.
Who is required to file annexure 4 participant informed?
Research investigators, project coordinators, and organizations involved in conducting studies that require participant consent are typically required to file Annexure 4 Participant Informed.
How to fill out annexure 4 participant informed?
To fill out Annexure 4 Participant Informed, one must provide details such as participant identification, study information, consent statement, and signatures of both the investigator and the participant.
What is the purpose of annexure 4 participant informed?
The purpose of Annexure 4 Participant Informed is to document that participants have been adequately informed about the study and have given their consent to participate, ensuring ethical standards are met.
What information must be reported on annexure 4 participant informed?
Information that must be reported includes participant details, study objectives, procedures, potential risks and benefits, and confirmation of informed consent.
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